50 Person ANSI

Manufacturer
Genuine First Aid LLC | GFA Production ( Xiamen) Co., Ltd
Effective date
2010-06-07
Label type
HUMAN OTC DRUG LABEL
Version
13
Source
full-release
Hydrated at
2026-05-31 22:24:46

Label at a glance#

Product50 Person ANSI
Active ingredientBENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL
Label structure120 sections

Storage and handling

Other Information: Store at room temperature

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:

Benzalkonium Chloride 0.13%
Lidocaine HCL 0.5%

OTC - PURPOSE SECTION

Purpose: First aid antiseptic, external analgesic

Uses: First aid to help prevent infection and for the temporary relief of pain and itching associated with:

Minor Cuts

Scrapes

Burns

WARNINGS SECTION

Warnings:

For external  use only

OTC - DO NOT USE SECTION

Do not use: In eyes, in large quantities, over raw blistered areas, or on deep puncture wounds, animal bites or serious burns, for more than one week

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of Children.

If ingested, contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions: Clean affected area, Apply small amount not more than 3 times daily.

May be covered with a sterile bandage.

STORAGE AND HANDLING SECTION

Other Information:

Store at room temperature

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Genuine First Aid Burn Cream

Antiseptic Pain Relief With Aloe

Net Wt 0.9g (1/32 oz)

Manufactured in CHINA for

Genuine First Aid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BurnCreamBurnCream

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:                                            Purpose

Benzalkonium Chloride 0.40%..........    First Aid Antiseptic

OTC - PURPOSE SECTION

Use: For Professional and Hospital use.  Helps prevent infection.  Antiseptic cleansing of face, hands and body without soap and water.

WARNINGS SECTION

Warning:    For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children:  If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use if unusual redness, swelling or other symptoms occur. Consult a physician immediately.

OTC - DO NOT USE SECTION

Do not use in the eyes or over large areas of the body.

OTC - WHEN USING SECTION

Directions: Tear open packet, unfold towelette and use to cleanse desired skin area.  Discard towelette appropriately after single use.

INACTIVE INGREDIENT SECTION

Inactive Ingredient:    Purified water

DESCRIPTION SECTION

LOT/EXP:                                    Made in CHINA

20130301

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antiseptic Towelette

Genuine First Aid LLC, Clearwater FL 33755

www.GenuineFirstAid.com

1/pouch

GENUINE FIRST AID

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antiseptic ToweletteAntiseptic Towelette

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: .........Bacitracin Zinc 400 units

Neomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)

Polymyxin B Sulfate 5000 units

OTC - PURPOSE SECTION

Uses:  To help prevent infection in:
minor cuts;  scrapes;  burns

WARNINGS SECTION

Warnings:

For external use only.

OTC - DO NOT USE SECTION

Do not use:  in eyes;  over large areas of the body;

If allergic to any of the ingredients;  for more than one week unless directed by a physician.

OTC - STOP USE SECTION

Stop use and consult a doctor:

if the condition persists or gets worse;  a rash or other allergic reaction develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If ingested, contact a Poison

Control Center right away.

OTC - WHEN USING SECTION

Directions: clean affected area;  apply small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily; may be covered with a sterile bandage

STORAGE AND HANDLING SECTION

Other information:

Store at room temperature.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Genuine Triple Antibiotic

First Aid Ointment

To Help Prevent Infection

Each Gram Contains:

Bacitracin Zinc 400 units

Neomycin Sulfate 5 mg

(equivalent to 3.5 mg

Neomycin base)

 Polymyxin B Sulfate 5000 units

Net Wt. 0.5g ; (1/64 oz)

Manufactured in CHINA for

GENUINE FIRST AID.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GenuineTripleAntibioticGenuineTripleAntibiotic

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Purified Water USP...q.s.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Sodium Chloride USP                                          44mg

Monobasic Sodium Phosphate USP                18mg
Sodium Phosphate Dibasic USP                       111mg  

Edetate Disodium USP                                       10mg

Benzalkonium Chloride                                      0.5mg
NF (as preservative)

STORAGE AND HANDLING SECTION

Store in a cool place. For irrigation only.

Discard unused portion of the solution.

Not for injection.

WARNINGS SECTION

Warning:

If you experience eye pain, changes in vision, continued redness or irritation of the eye,

or if the condition worsens or persists for more than 72 hours, discontinue use and consult a doctor.

Do not use if solution changes color or becomes cloudy.

DOSAGE & ADMINISTRATION SECTION


Directions

Remove contacts before using.

Twist top to remove.

Flush the affected area as needed. Control

Rate of flow by pressure on the bottle. Do not touch

tip of the container to any surface. Do not reuse.

If necessary continue flushing with emergency eyewash or shower.

Discard bottle after use.

OTC - PURPOSE SECTION

Uses:

For flushing or irrigating the eyes to

remove loose foreign material, air pollutants,

or chlorinated water.

DESCRIPTION SECTION

Code No.: GUJ/DRUG/G/1080

Batch No.:

Mfg Date:

Exp: Date:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10ml

Sterile Isotonic Buffered Genuine

 Eyewash

For single use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GenuineEyeWashGenuineEyeWash

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:                                    Purpose:

Benzocaine, 6% w/v..................    Topical Anesthetic

SD alcohol, 60% w/v..................    Antiseptic

OTC - PURPOSE SECTION

Use: For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

WARNINGS SECTION

Warnings: For external use only.

Avoid contact with eyes.  If this happens, rinse thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

STORAGE AND HANDLING SECTION

Flammable - keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use: In eyes, on broken skin, deep puncture wounds.  If unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately.

DESCRIPTION SECTION

Made in CHINA

LOT/EXP:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Insect Sting Relief Pad

Genuine First Aid LLC, Clearwater FL 33755
                        www.GenuineFirstAid.com

1/pouch

GENUINE FIRST AID

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Insect Sting Relief PadInsect Sting Relief Pad

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each tablet)                       Purpose

Ibuprofen USP (NSAID*) 200mg . . . . . . . . . . . .Pain reliever/fever reducer

*nonsteroidal anti-inflammatory drug

OTC - PURPOSE SECTION


Uses temporarily relieves minor aches and pains due to:

the common cold

headache

toothache

muscular aches

backache

minor pain of arthritis

menstrual cramps temporarily reduces fever

WARNINGS SECTION

Warnings

Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: shock,  facial swelling,  asthma (wheezing) rash, skin reddening, blisters, hives If an allergic reaction occurs, stop use and seek medical help right away.
Stomach bleeding warning: This product contains a nonsteroidal anti-inflammatory drug (NSAID), which may cause severe stomach
bleeding. The chance is higher if you: are age 60 or older, have had stomach ulcers or bleeding problems, take a blood thinner (anticoagulant) or steroid drug, take other drugs containing NSAIDs (aspirin, ibuprofen, naproxen, or others), have 3 or more alcoholic drinks every day while using this product, take more or for a longer time than directed

OTC - DO NOT USE SECTION


Do not use if you have ever had an allergic reaction to any other pain reliever/fever reducer,  right before or after heart surgery.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if  stomach bleeding warning applies to you; you have a history of stomach problems such as heartburn; you have a high blood pressure, heart disease, liver cirrhosis, or kidney disease; you are taking a diuretic

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor before use if you are:
taking any other drug containing NSAID (prescription or nonprescription); taking aspirin for heart attack or stroke, because Ibuprofen may decrease this benefit of aspirin; taking any other drug

OTC - WHEN USING SECTION

When using this product:
take with food or milk if stomach upset occurs

OTC - STOP USE SECTION

Stop use and ask a doctor If:
you experience any of the following signs of stomach bleeding; feel faint; vomit blood; have bloody or black stools; have stomach pain that does get better; pain gets worse or lasts more than 10 days; fever gets worse or lasts more than 3 days; redness or swelling is present in the painful area; any new symptoms appear

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use ibuprofen during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions:
do not use more than directed; the smallest effective dose should be used; do not take longer than 10 days, unless directed by a doctor.

Adults and Children (12 years and older):  Take 1 tablet every 4 to 6 hours while symptoms persist.  If pain or fever does not respond to 1 tablet, 2 tablets may be used.  Do not exceed 6 tablets in 24 hours, unless directed by a doctor.

Children under 12 years: Do not give to children under 12 years of age.

STORAGE AND HANDLING SECTION


Other information:  Store at controlled room temperature; avoid excessive heat 40 degree Celsius (104 degree Fahrenheit); tamper evident sealed packets; do not use any opened or torn packets

INACTIVE INGREDIENT SECTION

Inactive ingredients: cellulose, corn starch, fumed silica gel, hypromellose, lactose, magnesium stearate, polydextrose, polyethylene glycol, povidone, silica, sodium starch glycolate, stearic acid, titanium dioxide, triacetin.

DESCRIPTION SECTION

Distributed by GENUINE FIRST AID
600 Cleveland Str Suite 400, Clearwater, FL 33755

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IBUPROFEN 2 Tablets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IbuprofenIbuprofen

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each tablet)                Purpose

Acetaminophen 325 mg .............                Analgesic/antipyretic

OTC - PURPOSE SECTION

Uses

temporary relief of minor aches and pains associated with:

common cold;  headache; toothache; muscular aches;  backache; arthritis; menstrual cramps;  and reduction of fever

WARNINGS SECTION

Warnings:

Liver warning:    This product contains acetaminophen.

Severe liver damage may occur if:  adult takes more than 12 tablets in 24 hours, which is the maximum daily amount; child takes more than 5 doses in 24 hours;  taken with other drugs containing acetaminophen;  adult has 3 or more alcoholic drinks every day while using this product

OTC - DO NOT USE SECTION

Do not use:  with any other drug containing acetaminophen (prescription or nonprescription).  If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist;  for more than 10 days for pain unless directed by a doctor; for more than 3 days for fever unless directed by a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if the user has liver disease

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin

OTC - STOP USE SECTION

Stop use and ask a doctor if: symptoms do not improve; pain gets worse or lasts for more than 10 days; fever gets worse or lasts for more than 3 days; new symptoms occur;  redness or swelling is present; a rare sensitivity reaction occurs

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  In case of accidental overdose, contact a doctor or Poison Control Center immediately.  Prompt
medical attention is critical for adults as well as for children even if
you do not notice any signs or symptoms.  Do not exceed recommended dosage

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and Children                                Take 2 tablets every 4 to 6 hours as

12 years of age                                         needed.  Do not take more than 12 tablets

or older                                                        in 24 hours.


Children 6-11 years                                    Take 1 tablet every 4 to 6 hours as

of age                                                              needed.  Do not take more than 5

                                                                         tablets in 24 hours.


Children under 6                                          Do not use this regular strength product.

years of age                                                  This will provide more than the

                                                                          recommended dose (overdose) and could

                                                                          cause serious health problems.

STORAGE AND HANDLING SECTION

Store at 59-86 degree Farenheat (15-30 degree Celcius)

GENERAL PRECAUTIONS SECTION

tamper evident sealed packets; do not use any open or torn packets

DESCRIPTION SECTION

Distributed by GENUINE FIRST AID
600 Cleveland Str Suite 400, Clearwater, FL 33755

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GENUINE FIRST AID            2 Tablets

NON-ASPIRIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Non AspirinNon Aspirin

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each tablet)                             Purpose

Aspirin (NSAID*) 325 mg...............................   Pain Reliever / fever reducer

*nonsteroidal anti-inflammatory drug  

OTC - PURPOSE SECTION

Uses    Temporarily relieves minor aches and pains associated with:
headache ; muscular aches ; minor arthritis pain ; backache ; common cold ; toothache ; menstrual cramps ; Temporarily reduces fever

WARNINGS SECTION

Warnings

Reye's syndrome:  Children and teenagers who have or are recovering from chicken pox of flu-like symptoms should not use this product.  When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

Allergy alert:    Aspirin may cause a severe allergic reaction which may include:  hives, skin reddening, facial swelling, rash,  asthma (wheezing), blisters, shock, If an allergic reaction occurs, stop use and seek medical help right away.

Stomach bleeding warning:    This contains an NSAID, which may cause severe stomach bleeding.  The chance is higher if you:
are age 60 or older; have had stomach ulcers or bleeding problems; take a blood thinner (anticoagulant) or steroid drug; take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others); have 3 or more alcoholic drinks every day while using this product; take more or for a longer time than directed

OTC - DO NOT USE SECTION

Do not use:  if you have ever had an allergic reaction to any other pain reliever/ fever reducer; right before or after heart surgery; if you are taking a prescription drug for gout, diabetes or arthritis

OTC - ASK DOCTOR SECTION

Ask a doctor before use if: stomach bleeding warning applies to you;  you have a history of stomach problems such as heartburn; you have high blood pressure, heart disease, liver cirrhosis, or kidney disease; you are taking a diuretic

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are:

under a doctor's care for any serious condition;  taking any other drug

OTC - WHEN USING SECTION

When using this product: take with food or milk if stomach upset occurs

OTC - STOP USE SECTION


Stop use and ask a doctor if
you experience any of the following signs of stomach bleeding:
feel faint;  vomit blood; have bloody or black stools; have stomach
pain that does not get better; pain gets worse or lasts more than 10 days;  fever gets worse or lasts more than 3 days; you have difficulty swallowing; if ringing in the ears or loss of hearing occurs; redness or swelling is present in the painful areas; any new symptoms appear

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use. It is especially important to use aspirin during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  In case of overdose, get medical help or

contact a Poison Control Center right away.

OTC - WHEN USING SECTION

Directions

do not use more than directed

the smallest effective dose should be used

drink a full glass of water with each dose

do not take longer than 10 days, unless directed by a doctor

DOSAGE & ADMINISTRATION SECTION

Adults and children: (12 years and older) Take 1 or 2 tablets with

water every 4 hours as needed.  Do not take more than 12 tablets in 24

hours, or as directed by a doctor.

Children under 12 years:    Do not give to children under 12 years of age.

STORAGE AND HANDLING SECTION

Store at 59 - 86  degree Fahrenheit (15 - 30 degree Celsius); avoid

excessive heat and humidity;  tamper evident sealed packets;

Do not use any opened or torn packets

INACTIVE INGREDIENT SECTION

Inactive Ingredients:  hypromellose, polyethylene glycol, propylene glycol, corn starch

DESCRIPTION SECTION

Distributed by GENUINE FIRST AID
600 Clevelad Str Suite 400, Clearwater, FL 33755

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ASPIRIN 2 Tablets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aspirin 325mgAspirin 325mg

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:                                        Purpose

Isopropyl Alcohol, 70% v/v...............        Antiseptic

OTC - PURPOSE SECTION

Use:    For preparation of skin before injection.

WARNINGS SECTION

Warnings:    For external use only. 

STORAGE AND HANDLING SECTION

Flammable - keep away from fire or flame

Store at room temperature 15-30 degree Celsius (59-86 degree Fahrenheit)

OTC - DO NOT USE SECTION

Do not use: with electrocautery, in the eyes.

OTC - STOP USE SECTION

Stop use if irritation and redness develop. If condition persists for more than 72 hours, consult your doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

Wipe Injection site vigorously and discard.

INACTIVE INGREDIENT SECTION

Inactive Ingredient:    Purified water.

DESCRIPTION SECTION

LOT/EXP:                Made in CHINA

20140301

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol Cleansing  Pad
Genuine First Aid LLC, Clearwater FL 33755

www.GenuineFirstAid.com

1/pouch

GENUINE FIRST AID

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AlcoholCleansingPadAlcoholCleansingPad

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Ethyl Alcohol 62 percent

OTC - PURPOSE SECTION

Enter section text here

WARNINGS SECTION

Warnings:

For external use only

Flammable, keep away from fire or flame

OTC - DO NOT USE SECTION

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and consult a doctor if irritation and redness develop

and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions:

Empty contents into palm. Rub hands until gel dissipates. Recommended for repeated use.

STORAGE AND HANDLING SECTION

Other Information: Store at 15 to 25 degree Celsius  (59 to 77 degree Fahrenheit)

OTC - ACTIVE INGREDIENT SECTION

Genuine Hand Sanitizer

Instant Gel

Antiseptic Handwash

with Vitamin E and Aloe

Kills 99.9 percent of germs

Without Water

Active Ingredient:
Ethyl Alcohol 62 percent

Net Wt 0.9g (1/32 oz)

Manufactured in China For

Genuine First Aid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Genuine Hand SanitizerGenuine Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANSI/ISEA Z308.1-2009 TYPE III

Caution! This Kit meets ANSI/ISEA Z308.1-2009 only when required minimum fill
is maintained with first aid products marked "ANSI/ISEA Z308.1-2009."


CARRYING CASE
1 Easy Access Pocket System
1 Hard Case

POCKET 1: SMALL CUTS AND BURNS
100 Adhesive Plastic Bandages 1"x3"
2 Knuckle Fabric Bandage
25 Adhesive Spot Bandages 7/8"X7/8"
2 Fingertip
Fabric Bandage
2 Elbow Knee Adhesive Bandage
6 Burn Cream
15 Antiseptic
Towelettes
6 Triple Antibiotic Ointment 0.5gr
40 Cotton Tipped
Applicators

POCKET 2: MEDIUM CUTS AND SCRATCHES
15 Antiseptic
Towelettes
4 Sterile Gauze Pad 3"x3"
4 Sterile Gauze Pads 4"X4"
2
Roller Gauze Bandage 2"X4.1yds
1 Roller Gauze Bandage 3"X4.1yds
2 Sterile
Eye Pads
2 Sterile Eye Wash 10ml Twist Top
1 Butterfly Wound Closure,
Medium

POCKET 3: SEVERE BLEEDING AND BURNS
2 First Aid Tape Rolls 1/2"x5 yds.
2 Combine Pad 5"X9"

POCKET 4: CPR
1 CPR Breathing Barrier

POCKET 5: PROTECTION
4
Medical Grade Vinyl Gloves
1 Instant Cold Compress
30 Alcohol Cleansing
Pads
1 Hand Sanitizer 0.9g
2 Insect Sting Relief Pads
2 Triangular
Bandage 42"x42"x59"
2 Ibuprofen 200mg
2 Non Aspirin 325mg
4 Aspirin
325mg

POCKET 6: INSTRUMENTS
1 Emergency First Aid Guide
1 Plastic
Tweezers
1 Scissors



Manufactured in China for:

Genuine
First Aid LLC.
600 Cleveland Street
Suite 400
Clearwater FL
33755

www.GenuineFirstAid.com

GENUINE FIRST AID

Copyright c 2010 Genuine First Aid LLC. All rights reserved.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANSI Kit 50 PersonsANSI Kit 50 Persons

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313782acetaminophen 325 MG Oral TabletPSN13
212033aspirin 325 MG Oral TabletPSN13
204602bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical OintmentPSN13
1012100benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical CreamPSN13
1038561benzalkonium Cl 0.4 % Medicated PadPSN13
1046313benzocaine 6 % / ethanol 60 % Medicated PadPSN13
581660ethanol 62 % Topical GelPSN13
310965ibuprofen 200 MG Oral TabletPSN13
797544isopropyl alcohol 70 % Medicated PadPSN13
1053490water 98.16 % Ophthalmic Irrigation SolutionPSN13
313782acetaminophen 325 MG Oral TabletSCD13
212033aspirin 325 MG Oral TabletSCD13
204602bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical OintmentSCD13
1012100benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical CreamSCD13
1038561benzalkonium chloride 4 MG/ML Medicated PadSCD13
1046313benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated PadSCD13
581660ethanol 0.62 ML/ML Topical GelSCD13
310965ibuprofen 200 MG Oral TabletSCD13
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD13
1053490water 982 MG/ML Ophthalmic Irrigation SolutionSCD13
313782APAP 325 MG Oral TabletSY13
212033ASA 325 MG Oral TabletSY13
204602bacitracin 400 UNT / neomycin 3.5 MG (as neomycin sulfate 5 MG) / polymyxin B 5000 UNT per GM Topical OintmentSY13
1012100benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical CreamSY13
1038561benzalkonium chloride 0.4 % Medicated ToweletteSY13
1038561benzalkonium chloride 0.4 % Topical SwabSY13
1046313benzocaine 6 % / ethanol 60 % Topical SwabSY13
581660ethanol 62 % Topical GelSY13
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY13
797544isopropyl alcohol 70 % Medicated PadSY13
797544isopropyl alcohol 70 % Topical ClothSY13
797544isopropyl alcohol 70 % Topical SwabSY13
1053490water 98.16 % Ophthalmic Irrigation SolutionSY13
1053490water 98.16 ML per 100 ML Ophthalmic Irrigation SolutionSY13

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ASPIRIN Pharmacologic Class Indexing3Indexing - Pharmacologic Class20191108
BACITRACIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
BENZOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
IBUPROFEN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20191108
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
NEOMYCIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
POLYMYXIN B Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
16cde546-8deb-4df2-a072-dab5566ede95Product name120231003
f6d1b8d7-3bd1-4248-eddd-b60565c88015Product name420230808
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
874f4e63-49d2-5150-5d77-052172814ebdProduct name620230105
d7724692-1155-4cc8-a415-22f5fc4aec35Product name620220216
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
bde672ba-4805-28d0-1986-73543d41b412Product name220210201
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
ade821ba-260a-47e2-bd89-743e27ac9906Product name120161121
99e684e6-f435-feb8-d2bb-3a546f1cb768Product name220161117
557673c2-8256-b351-e863-4ec71a5a64b0Product name220160714
25340b3b-3e4c-4ff8-abf6-3e62ec46bd0cProduct name120160603
dbc9a339-6215-4e94-9546-57a3b34902ceProduct name120160517
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
9425d234-4ae1-4b53-adc6-8cc7af6dd657Product name120150929
2d352c73-a357-4193-a4de-dfdf9a2ac8e4Product name120150819
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
2a21311a-89e2-0e83-2ebd-117f9798b2b2Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
61c18d4e-b552-5478-8fc0-df38b93e3100Product name120140508
7b2938c9-7eb7-e312-ae90-f54f4240361eProduct name120140508
9007e8a7-ff50-f9b9-7945-f2a1deadd94eProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
997601aa-bb5f-6971-6b90-a21132c12c7bProduct name120140508
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
b6082387-f592-1148-0844-bd068fd213fbProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52124-0113-12020-01-31C16284748780-19d75b9d1-0c81-f424-e053-dadaa90a57ce50 Person ANSI

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52124-0001-150 Person ANSI0.8 mL in 1 PACKAGELIQUID24 mL0.40 mL in 100mL13
52124-0002-150 Person ANSI0.5 mL in 1 PACKAGELIQUID15 mL70 mL in 100mL13
52124-0003-150 Person ANSI0.5 g in 1 TUBEOINTMENT3 g5000 [iU] in 1g13
52124-0004-150 Person ANSI0.9 g in 1 PACKAGECREAM5.4 g0.5 g in 100g13
52124-0005-150 Person ANSI10 mL in 1 BOTTLELIQUID20 mL98.16 mL in 100mL13
52124-0006-150 Person ANSI0.9 g in 1 PACKAGEGEL0.9 g62 g in 100g13
52124-0008-150 Person ANSI0.5 mL in 1 PACKAGELIQUID1 mL60 mL in 100mL13
52124-0009-150 Person ANSI2 in 1 PACKAGETABLET2200 mg13
52124-0010-150 Person ANSI2 in 1 PACKAGETABLET2325 mg13
52124-0011-150 Person ANSI2 in 1 PACKAGETABLET4325 mg13
52124-0113-150 Person ANSI1 in 1 KITKIT113

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52124-000150 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-000250 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-000350 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-000450 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-000550 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-000650 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-000850 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-000950 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-001050 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-001150 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip
52124-011350 PERSON ANSI (BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, WATER, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN, ISOPROPYL ALCOHOL) KIT [GENUINE FIRST AID LLC]13Legacy NDC, 11 package rows20100610_6bd126f0-967e-47d2-82d8-1c90f69aca5d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9D13
ALCOHOLACTIVE INGREDIENT3K9958V90M13
ASPIRINACTIVE INGREDIENTR16CO5Y76E13
BACITRACIN ZINCACTIVE INGREDIENT89Y4M234ES13
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W713
BENZOCAINEACTIVE INGREDIENTU3RSY48JW513
IBUPROFENACTIVE INGREDIENTWK2XYI10QM13
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M41630213
LIDOCAINEACTIVE INGREDIENT98PI20098713
NEOMYCIN SULFATEACTIVE INGREDIENT057Y62669313
POLYMYXIN B SULFATEACTIVE INGREDIENT19371312D413
WATERACTIVE INGREDIENT059QF0KO0R13
ACETAMINOPHENACTIVE MOIETY362O9ITL9D13
ALCOHOLACTIVE MOIETY3K9958V90M13
ASPIRINACTIVE MOIETYR16CO5Y76E13
BACITRACINACTIVE MOIETY58H6RWO52I13
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y13
BENZOCAINEACTIVE MOIETYU3RSY48JW513
IBUPROFENACTIVE MOIETYWK2XYI10QM13
ISOPROPYL ALCOHOLACTIVE MOIETYND2M41630213
LIDOCAINEACTIVE MOIETY98PI20098713
NEOMYCINACTIVE MOIETYI16QD7X29713
POLYMYXIN BACTIVE MOIETYJ2VZ07J96K13
WATERACTIVE MOIETY059QF0KO0R13
BENZALKONIUM CHLORIDEINACTIVE INGREDIENTF5UM2KM3W713
EDETATE DISODIUMINACTIVE INGREDIENT7FLD91C86K13
HYPROMELLOSEINACTIVE INGREDIENT3NXW29V3WO13
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G13
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I3013
POLYDEXTROSEINACTIVE INGREDIENTVH2XOU12IE13
POLYETHYLENE GLYCOLINACTIVE INGREDIENT3WJQ0SDW1A13
POVIDONEINACTIVE INGREDIENTFZ989GH94E13
POWDERED CELLULOSEINACTIVE INGREDIENTSMD1X3XO9M13
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU413
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8X13
SODIUM PHOSPHATE, DIBASICINACTIVE INGREDIENTGR686LBA7413
SODIUM PHOSPHATE, MONOBASICINACTIVE INGREDIENT3980JIH2SW13
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJ13
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65AP13
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JP13
TRIACETININACTIVE INGREDIENTXHX3C3X67313
WATERINACTIVE INGREDIENT059QF0KO0R13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 45 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 40 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 10 · 560 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / PERINEURAL648 mgExact identifier — unii candidate
134 equally ranked IID candidates
TRIACETINTRIACETINXHX3C3X673CONCENTRATE / ORAL250 mgExact identifier — unii candidate
14 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJINSERT / VAGINAL147 mgExact identifier — unii candidate
22 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4POWDER / RESPIRATORY (INHALATION)NAExact identifier — unii candidate
49 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4TABLET, EXTENDED RELEASE / ORAL450 mgExact identifier — unii candidate
49 equally ranked IID candidates
HYPROMELLOSEHYPROMELLOSE3NXW29V3WOLOTION / TOPICAL0.1 %w/wExact identifier — unii candidate
27 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRAVENOUS28773 mgExact identifier — unii candidate
134 equally ranked IID candidates
TRIACETINTRIACETINXHX3C3X673SUSPENSION / ORAL7 mgExact identifier — unii candidate
14 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KTABLET, CHEWABLE / ORAL1 mgExact identifier — unii candidate
77 equally ranked IID candidates
POWDERED CELLULOSEPOWDERED CELLULOSESMD1X3XO9MTABLET / SUBLINGUAL4.5 mgExact identifier — unii candidate
16 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, SUGAR COATED / ORALNAExact identifier — unii candidate
36 equally ranked IID candidates
TRIACETINTRIACETINXHX3C3X673CAPSULE, DELAYED RELEASE / ORAL5.1 mgExact identifier — unii candidate
14 equally ranked IID candidates
HYPROMELLOSEHYPROMELLOSE3NXW29V3WOCAPSULE, COATED PELLETS / ORAL3.32 mgExact identifier — unii candidate
27 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4GEL / TOPICAL6 mgExact identifier — unii candidate
49 equally ranked IID candidates
SODIUM PHOSPHATE, DIBASICSODIUM PHOSPHATE, DIBASICGR686LBA74INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS40 mgExact identifier — unii candidate
14 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30WAFER / ORAL66 mgExact identifier — unii candidate
39 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4TABLET, FILM COATED, EXTENDED RELEASE / ORAL336 mgExact identifier — unii candidate
49 equally ranked IID candidates
POWDERED CELLULOSEPOWDERED CELLULOSESMD1X3XO9MPOWDER, FOR SUSPENSION / ORAL1600 mgExact identifier — unii candidate
16 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, CHEWABLE / ORAL1412 mgExact identifier — unii candidate
36 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUPPOSITORY / RECTAL140 mgExact identifier — unii candidate
134 equally ranked IID candidates
POWDERED CELLULOSEPOWDERED CELLULOSESMD1X3XO9MPASTE, DENTIFRICE / DENTALNAExact identifier — unii candidate
16 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30GRANULE / ORAL629 mgExact identifier — unii candidate
39 equally ranked IID candidates
STEARIC ACIDSTEARIC ACID4ELV7Z65APTABLET, ORALLY DISINTEGRATING / ORAL10 mgExact identifier — unii candidate
26 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPSUPPOSITORY, EXTENDED RELEASE / INTRAUTERINE1 mgExact identifier — unii candidate
40 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPGRANULE, FOR SUSPENSION / ORAL143 mgExact identifier — unii candidate
40 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, DELAYED RELEASE / ORAL713 mgExact identifier — unii candidate
22 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KSUSPENSION / OPHTHALMIC0.06 %w/vExact identifier — unii candidate
77 equally ranked IID candidates
HYPROMELLOSEHYPROMELLOSE3NXW29V3WOSHAMPOO / TOPICAL3 %w/wExact identifier — unii candidate
27 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPFILM, SOLUBLE / ORAL2 mgExact identifier — unii candidate
40 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KINJECTION, EMULSION / INTRAVENOUS59 mgExact identifier — unii candidate
77 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRACAUDAL210 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XGRANULE, FOR SUSPENSION / ORAL162 mgExact identifier — unii candidate
134 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30LOZENGE / ORAL420 mgExact identifier — unii candidate
39 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XDROPS / ORALNAExact identifier — unii candidate
134 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KINJECTION / INTRACARDIAC2 mgExact identifier — unii candidate
77 equally ranked IID candidates
BENZALKONIUM CHLORIDEBENZALKONIUM CHLORIDEF5UM2KM3W7LIQUID / NASAL0.2 mg/1mlExact identifier — unii candidate
24 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4TABLET / SUBLINGUAL10 mgExact identifier — unii candidate
49 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30CREAM / TOPICALNAExact identifier — unii candidate
39 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KTABLET, COATED / ORAL0.21 mgExact identifier — unii candidate
77 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL42 mgExact identifier — unii candidate
40 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSOLUTION / NASAL330 mgExact identifier — unii candidate
134 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GPOWDER, FOR SOLUTION / ORALNAExact identifier — unii candidate
36 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XPOWDER, FOR SUSPENSION / ORAL98 mgExact identifier — unii candidate
134 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KTABLET, ORALLY DISINTEGRATING / ORAL3 mgExact identifier — unii candidate
77 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUSPENSION/ DROPS / TOPICAL0.23 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, FILM COATED / ORAL590 mgExact identifier — unii candidate
36 equally ranked IID candidates
BENZALKONIUM CHLORIDEBENZALKONIUM CHLORIDEF5UM2KM3W7SOLUTION/ DROPS / AURICULAR (OTIC)0 %w/vExact identifier — unii candidate
24 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KINJECTION / SUBCUTANEOUS6 mgExact identifier — unii candidate
77 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XTABLET, FILM COATED / ORAL100 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / SUBMUCOSAL17 mgExact identifier — unii candidate
134 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii candidate
39 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KCAPSULE / ORAL5 mgExact identifier — unii candidate
77 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL21 mgExact identifier — unii candidate
22 equally ranked IID candidates
STEARIC ACIDSTEARIC ACID4ELV7Z65APCREAM / TOPICAL190 mgExact identifier — unii candidate
26 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION, CONCENTRATE / INTRAVENOUS0.86 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GGRANULE, FOR SUSPENSION / ORAL512.5 mg/5mlExact identifier — unii candidate
36 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION / INTRADERMAL7 mgExact identifier — unii candidate
134 equally ranked IID candidates
BENZALKONIUM CHLORIDEBENZALKONIUM CHLORIDEF5UM2KM3W7SUSPENSION/ DROPS / TOPICALNAExact identifier — unii candidate
24 equally ranked IID candidates
SODIUM PHOSPHATE, MONOBASICSODIUM PHOSPHATE, MONOBASIC3980JIH2SWINJECTION, POWDER, FOR SOLUTION / INTRAVENOUS13.2 mgExact identifier — unii candidate
9 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJCAPSULE / ORAL5785 mgExact identifier — unii candidate
22 equally ranked IID candidates

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A075010-001IBUPROFENIBUPROFEN200MGTABLET / ORAL1999-03-01

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 44 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-10-15 13:18:302026-09A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01c2088c7a36db…
2026-09-14 22:38:342026-08A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-0184e616aacf4f…
2026-08-18 06:07:402026-07A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-0131067a03dcf5…
2025-08-23 18:47 UTC2025-08A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-016a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-0103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-012680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-015bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-0179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-011e350fbaab3a…
2024-05-31 18:47 UTC2024-05A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-018072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-015c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-015d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-014b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-0174a2ff9319b5…
2022-03-09 01:35 UTC2022-03A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-0187673890dc5c…
2021-03-12 10:30 UTC2021-03A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-015aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-018869cabd3fbd…
2020-11-12 02:37 UTC2020-11A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01c0c555d07b60…
2019-12-14 00:12 UTC2019-12A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-013f01610625f2…
2019-09-15 20:21 UTC2019-09A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01b00525d2431f…
2019-07-19 19:46 UTC2019-07A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01ea99ee380514…
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2024-02-18 07:12 UTC2024-02A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-011c564ffb4f44…
2023-12-20 04:57 UTC2023-12A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01ea1830bbd6c7…
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2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-019b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-013f0d92c62455…
2023-05-13 08:27 UTC2023-05A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-01053a50430f4f…
2023-01-26 05:58 UTC2023-01A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-013bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A075010-001IBUPROFEN200MGTABLET / ORAL1999-03-013a93d1ddd44b…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2a883d44-4542-4a0e-8202-6a70e159ee526bd126f0-967e-47d2-82d8-1c90f69aca5d2010-06-07WarningsExact identifier
spl id: 2a883d44-4542-4a0e-8202-6a70e159ee52
spl set id: 6bd126f0-967e-47d2-82d8-1c90f69aca5d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.