Indications and uses
Provides, antiseptic germicidal skin preperation for minor invasive procedures
Provides, antiseptic germicidal skin preperation for minor invasive procedures
Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.
Other information: Store at room temperature.
Active Ingredient:
Benzalkonium Chloride 0.40%
For Professional and Hospital use. Helps prevent infection. Antiseptic cleansing of face, hands and body without soap and water.
Warning: For external use only.
Keep out of reach of children: If swallowed, get medical help or contact a Poison Control Center right away.
Stop use if unusual redness, swelling or other symptoms occur. Consult a physician immediately.
Do not use in the eyes or over large areas of the body.
Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.
Inactive Ingredient: Purified water
LOT/EXP: Made in CHINA
20130301
Antiseptic Towelette
Genuine First Aid LLC, Clearwater FL 33755
1/pouch
GENUINE FIRST AID
Active Ingredient: .........Bacitracin Zinc 400 units
Neomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)
Polymyxin B Sulfate 5000 units
Triple Antibiotic
Uses: To help prevent infection in:
minor cuts; scrapes; burns
For external use only.
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.
Stop use and consult a doctor:
if the condition persists or gets worse; a rash or other allergic reaction develops
Keep out of reach of children.
If ingested, contact a Poison
Control Center right away.
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
Other information:
Store at room temperature.
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.
Triple Antibiotic Ointment 10pcs
Net wt. 0.9g (1/32oz)
100
Triple Antibiotic
One Prep pad saturated with a 10% Povidone-Iodine solution equivalent to 1% available iodine
antiseptic, germicidal
Provides, antiseptic germicidal skin preperation for minor invasive procedures
For external use only.
In case of deep or puncture wounds or serious burns, and if pain, irritation, redness, swelling or infection occurs, discontinue use and contact a physician.
Purified water.
Clean intended area thoroughly with pad. Discard after single use.
Ethyl Alcohol 62%
Antimicrobial
For handwashing to decrease bacteria on the skin.
For external use only.
Flammable
in the eyes. In case of contact, rinse eyes thoroughly with water.
Empty contents into palm. Rub hands until gel dissipates. Recommended for repeated use.
Propylene glycol, carbomer, titanium dioxide, purified water
If swallowed, get medical help or contact a Poison Control Center right away.
Genuine Hand Sanitizer
Instant Gel
Antiseptic Handwash with Vitamin E and Aloe
Kills 99.9% of germs without water
Active Ingredient:
Ethyl alcohol 62%
Net Wt 0.9g (1/32oz)
ACTIVE INGREDIENTS:
Benzalkonium Chloride 0.13%
Lidocaine HCL 0.5%
Purpose: First aid antiseptic, external analgesic
First aid to help prevent infection and for the temporary relief of pain and itching associated with:
Minor Cuts
Scrapes
Burns
Keep out of reach of Children.
If ingested, contact a Poison Control Center right away.
Adults and children 2 years of age and older
clean affected area.
apply a small amount of this product on the area 1 to 3 times daily.
may be covered with a sterile bandage
children under 2 years of age: consult a doctor
Other Information:
Store at room temperature (do not freeze).
Taper evident sealed packets.
Do not use packet if opened or torn.
Aloe vera, cetyl alcohol, diazolidinyl urea, edetate disodium, glycerin, glyceryl monostearate, methylparaben, mineral oil, polyethylene glycol, propylene glycol, propylparaben, purified water, stearic acid, irolamine
LOT/EXP: Made in CHINA
20130301
GFA Production Xiamen Co., Ltd
No. 20 Huli Industrial Park, Meixi Road, Tong'an, Xiamen, Fujian, China 361100
Tel: 86-592-7269515 Fax: 86-592-7269528 Http: //
www.gfaproduction.com
Genuine First Aid Burn Cream
Antiseptic Pain Relief With Aloe
Net Wt 0.9g (1/32 oz)
Manufactured in CHINA for
Genuine First Aid.
Ibuprofen USP (NSAID*) 200mg
*nonsteroidal anti-inflammatory drug
cellulose, corn starch, fumed silica gel, hypromellose, lactose, magnesium stearate, polydextrose, polyethylene glycol, povidone, silica, sodium starch glycolate, stearic acid, titanium dioxide, triacetin.
Distributed by GENUINE FIRST AID
600 Cleveland Str Suite 400, Clearwater, FL 33755
IBUPROFEN 2 Tablets
IBUPROFEN 2 Tablets
Acetaminophen 325 mg
temporary relief of minor aches and pains associated with:
common cold; headache; toothache; muscular aches; backache; arthritis; menstrual cramps; and reduction of fever
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
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
Ask a doctor before use if the user has liver disease
Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin
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
If pregnant or breast-feeding, ask a health professional before use.
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
Cornstarch, polyethylene glycol, stearic acid, povidone
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.
Store at 59-86 degree F (15-30 degree C)
tamper evident sealed packets; do not use any open or torn packets
GENUINE FIRST AID 2 Tablets
NON-ASPIRIN
Aspirin (NSAID*) 325 mg
*nonsteroidal anti-inflammatory drug
Pain Reliever / fever reducer
Temporarily relieves minor aches and pains associated with:
headache ; muscular aches ; minor arthritis pain ; backache ; common cold ; toothache ; menstrual cramps ; Temporarily reduces fever
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
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
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
Ask a doctor or pharmacist before use if you are:
under a doctor's care for any serious condition; taking any other drug
When using this product: take with food or milk if stomach upset occurs
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.
Keep out of reach of children. In case of overdose, get medical help or
contact a Poison Control Center right away.
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
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.
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
hypromellose, polyethylene glycol, propylene glycol, corn starch
Active Ingredient:
Purified Water USP...q.s.
Inactive Ingredients:
Sodium Chloride USP 44mg
Monobasic Sodium Phosphate USP 18mg
Sodium Phosphate Dibasic USP 111mgStore in a cool place. For irrigation only.
Discard unused portion of the solution.
Not for injection.
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.
Code No.: GUJ/DRUG/G/1080
Batch No.:
Mfg Date:
Exp: Date:
10ml
Sterile Isotonic Buffered Genuine
Eyewash
For single use only
Active Ingredient:
Isopropyl Alcohol, 70% v/v
Antiseptic
For preparation of skin before injection.
For external use only.
Flammable - keep away from fire or flame
Store at room temperature 15-30 degree Celsius (59-86 degree Fahrenheit)
Do not use: with electrocautery, in the eyes.
Stop use if irritation and redness develop. If condition persists for more than 72 hours, consult your doctor.
Keep out of reach of children. If swallowed,
get medical help or contact a Poison Control
Center right away.
Purified water.
LOT/EXP: Made in CHINA
20140301
Alcohol Cleansing Pad
Genuine First Aid LLC, Clearwater FL 337551/pouch
GENUINE FIRST AID
100 Alcohol cleansing pads
Reorder GFAP-39-02
Active Ingredient: Purpose:
Benzocaine, 6% w/v
SD alcohol, 60% w/v
Use: For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites.
Clean intended area thoroughly with pad. Discard after single use.
Warnings: For external use only.
Avoid contact with eyes. If this happens, rinse thoroughly with water.
If swallowed, get medical help or contact a Poison Control Center right away.
Purified water
Flammable - keep away from fire or flame.
Do not use: In eyes, on broken skin, deep puncture wounds. If unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately.
Made in CHINA
LOT/EXP:
Insect Sting Relief Pad
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 313782 | acetaminophen 325 MG Oral Tablet | PSN | 3 |
| 212033 | aspirin 325 MG Oral Tablet | PSN | 3 |
| 204602 | bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical Ointment | PSN | 3 |
| 1012100 | benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream | PSN | 3 |
| 1038561 | benzalkonium Cl 0.4 % Medicated Pad | PSN | 3 |
| 1046313 | benzocaine 6 % / ethanol 60 % Medicated Pad | PSN | 3 |
| 581660 | ethanol 62 % Topical Gel | PSN | 3 |
| 310965 | ibuprofen 200 MG Oral Tablet | PSN | 3 |
| 797544 | isopropyl alcohol 70 % Medicated Pad | PSN | 3 |
| 797730 | povidone-iodine 10 % Medicated Pad | PSN | 3 |
| 1053490 | water 98.16 % Ophthalmic Irrigation Solution | PSN | 3 |
| 313782 | acetaminophen 325 MG Oral Tablet | SCD | 3 |
| 212033 | aspirin 325 MG Oral Tablet | SCD | 3 |
| 204602 | bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment | SCD | 3 |
| 1012100 | benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream | SCD | 3 |
| 1038561 | benzalkonium chloride 4 MG/ML Medicated Pad | SCD | 3 |
| 1046313 | benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated Pad | SCD | 3 |
| 581660 | ethanol 0.62 ML/ML Topical Gel | SCD | 3 |
| 310965 | ibuprofen 200 MG Oral Tablet | SCD | 3 |
| 797544 | isopropyl alcohol 0.7 ML/ML Medicated Pad | SCD | 3 |
| 797730 | povidone-iodine 100 MG/ML Medicated Pad | SCD | 3 |
| 1053490 | water 982 MG/ML Ophthalmic Irrigation Solution | SCD | 3 |
| 313782 | APAP 325 MG Oral Tablet | SY | 3 |
| 212033 | ASA 325 MG Oral Tablet | SY | 3 |
| 204602 | bacitracin 400 UNT / neomycin 3.5 MG (as neomycin sulfate 5 MG) / polymyxin B 5000 UNT per GM Topical Ointment | SY | 3 |
| 1012100 | benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream | SY | 3 |
| 1038561 | benzalkonium chloride 0.4 % Medicated Towelette | SY | 3 |
| 1038561 | benzalkonium chloride 0.4 % Topical Swab | SY | 3 |
| 1046313 | benzocaine 6 % / ethanol 60 % Topical Swab | SY | 3 |
| 581660 | ethanol 62 % Topical Gel | SY | 3 |
| 310965 | ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral Tablet | SY | 3 |
| 797544 | isopropyl alcohol 70 % Medicated Pad | SY | 3 |
| 797544 | isopropyl alcohol 70 % Topical Cloth | SY | 3 |
| 797544 | isopropyl alcohol 70 % Topical Swab | SY | 3 |
| 797730 | povidone-iodine 10 % (titratable iodine 1 % ) Medicated Pad | SY | 3 |
| 797730 | povidone-iodine 10 % Medicated Pad | SY | 3 |
| 797730 | povidone-iodine 10 % Medicated Swabstick | SY | 3 |
| 1053490 | water 98.16 % Ophthalmic Irrigation Solution | SY | 3 |
| 1053490 | water 98.16 ML per 100 ML Ophthalmic Irrigation Solution | SY | 3 |
| Class | Version | Type | Effective |
|---|---|---|---|
| ASPIRIN Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20191108 |
| BACITRACIN Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| BENZOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| IBUPROFEN Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20191108 |
| LIDOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| NEOMYCIN Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| POLYMYXIN B Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52124-1154-1 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-d4e1-8e05-e053-dbdaa90a074a | GFA First Aid Kit |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52124-0001-1 | GFA First Aid75 Person Metal Case | 0.8 mL in 1 PACKAGE | SWAB | 40.0 mL | 0.4 mL in 100mL | 3 |
| 52124-0002-1 | GFA First Aid75 Person Metal Case | 0.5 mL in 1 PACKAGE | LIQUID | 15 mL | 70 mL in 100mL | 3 |
| 52124-0003-1 | GFA First Aid75 Person Metal Case | 0.5 g in 1 TUBE | OINTMENT | 5.0 g | 5000 [iU] in 1g | 3 |
| 52124-0004-1 | GFA First Aid75 Person Metal Case | 0.9 g in 1 PACKET | CREAM | 10.8 g | 0.13 g in 100g | 3 |
| 52124-0005-1 | GFA First Aid75 Person Metal Case | 10 mL in 1 BOTTLE | LIQUID | 20 mL | 98.16 mL in 100mL | 3 |
| 52124-0008-1 | GFA First Aid75 Person Metal Case | 0.5 mL in 1 PACKAGE | SWAB | 6 mL | 6 mL in 100mL | 3 |
| 52124-0009-1 | GFA First Aid75 Person Metal Case | 2 in 1 PACKET | TABLET | 4 | 200 mg | 3 |
| 52124-0010-1 | GFA First Aid75 Person Metal Case | 2 in 1 PACKAGE | TABLET | 4 | 325 mg | 3 |
| 52124-0011-1 | GFA First Aid75 Person Metal Case | 2 in 1 PACKAGE | TABLET | 8 | 325 mg | 3 |
| 52124-1154-1 | GFA First Aid75 Person Metal Case | 1 in 1 KIT | KIT | 1 | 3 | |
| 52124-2906-1 | GFA First Aid75 Person Metal Case | 0.9 g in 1 PACKET | GEL | 4.5 g | 62 g in 100g | 3 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52124-0001 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-0002 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-0003 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-0004 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-0005 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-0008 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-0009 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-0010 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-0011 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-1154 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC, 11 package rows | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-2901 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| 52124-2906 | GFA FIRST AID (BENZALKONIUM CHLORIDE, BENZALKONIUM CHLORIDE, LIDOCAINE, BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE, POVIDONE-IODINE, WATER, ALCOHOL, ASPIRIN, IBUPROFEN, ACETAMINOPHEN, BENZOCAINE, ALCOHOL) KIT [GENUINE FIRST AID, LLC] | 3 | Legacy NDC | 20110517_fa23be25-61c3-491c-b9e6-a5275c9bdc13.zip |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ACETAMINOPHEN | ACTIVE INGREDIENT | 362O9ITL9D | 3 | |
| ALCOHOL | ACTIVE INGREDIENT | 3K9958V90M | 3 | |
| ASPIRIN | ACTIVE INGREDIENT | R16CO5Y76E | 3 | |
| BACITRACIN ZINC | ACTIVE INGREDIENT | 89Y4M234ES | 3 | |
| BENZALKONIUM CHLORIDE | ACTIVE INGREDIENT | F5UM2KM3W7 | 3 | |
| BENZOCAINE | ACTIVE INGREDIENT | U3RSY48JW5 | 3 | |
| IBUPROFEN | ACTIVE INGREDIENT | WK2XYI10QM | 3 | |
| ISOPROPYL ALCOHOL | ACTIVE INGREDIENT | ND2M416302 | 3 | |
| LIDOCAINE | ACTIVE INGREDIENT | 98PI200987 | 3 | |
| NEOMYCIN SULFATE | ACTIVE INGREDIENT | 057Y626693 | 3 | |
| POLYMYXIN B SULFATE | ACTIVE INGREDIENT | 19371312D4 | 3 | |
| POVIDONE-IODINE | ACTIVE INGREDIENT | 85H0HZU99M | 3 | |
| WATER | ACTIVE INGREDIENT | 059QF0KO0R | 3 | |
| ACETAMINOPHEN | ACTIVE MOIETY | 362O9ITL9D | 3 | |
| ALCOHOL | ACTIVE MOIETY | 3K9958V90M | 3 | |
| ASPIRIN | ACTIVE MOIETY | R16CO5Y76E | 3 | |
| BACITRACIN | ACTIVE MOIETY | 58H6RWO52I | 3 | |
| BENZALKONIUM | ACTIVE MOIETY | 7N6JUD5X6Y | 3 | |
| BENZOCAINE | ACTIVE MOIETY | U3RSY48JW5 | 3 | |
| IBUPROFEN | ACTIVE MOIETY | WK2XYI10QM | 3 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | 3 | |
| ISOPROPYL ALCOHOL | ACTIVE MOIETY | ND2M416302 | 3 | |
| LIDOCAINE | ACTIVE MOIETY | 98PI200987 | 3 | |
| NEOMYCIN | ACTIVE MOIETY | I16QD7X297 | 3 | |
| POLYMYXIN B | ACTIVE MOIETY | J2VZ07J96K | 3 | |
| WATER | ACTIVE MOIETY | 059QF0KO0R | 3 | |
| ALOE VERA LEAF | INACTIVE INGREDIENT | ZY81Z83H0X | 3 | |
| BENZALKONIUM CHLORIDE | INACTIVE INGREDIENT | F5UM2KM3W7 | 3 | |
| CETYL ALCOHOL | INACTIVE INGREDIENT | 936JST6JCN | 3 | |
| DIAZOLIDINYL UREA | INACTIVE INGREDIENT | H5RIZ3MPW4 | 3 | |
| EDETATE DISODIUM | INACTIVE INGREDIENT | 7FLD91C86K | 3 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | 3 | |
| GLYCERYL MONOSTEARATE | INACTIVE INGREDIENT | 230OU9XXE4 | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | 3 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | 3 | |
| METHYLPARABEN | INACTIVE INGREDIENT | A2I8C7HI9T | 3 | |
| MINERAL OIL | INACTIVE INGREDIENT | T5L8T28FGP | 3 | |
| POLYDEXTROSE | INACTIVE INGREDIENT | VH2XOU12IE | 3 | |
| POLYETHYLENE GLYCOL | INACTIVE INGREDIENT | 3WJQ0SDW1A | 3 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | 3 | |
| POWDERED CELLULOSE | INACTIVE INGREDIENT | SMD1X3XO9M | 3 | |
| PROPYLENE GLYCOL | INACTIVE INGREDIENT | 6DC9Q167V3 | 3 | |
| PROPYLPARABEN | INACTIVE INGREDIENT | Z8IX2SC1OH | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | 3 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | 3 | |
| SODIUM PHOSPHATE, DIBASIC | INACTIVE INGREDIENT | GR686LBA74 | 3 | |
| SODIUM PHOSPHATE, MONOBASIC | INACTIVE INGREDIENT | 3980JIH2SW | 3 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | 3 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | 3 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | 3 | |
| TRIACETIN | INACTIVE INGREDIENT | XHX3C3X673 | 3 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 3 |
Every source-derived product name is available through these pages.
Every source-derived ingredient row is available through these pages.
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | SUSPENSION/ DROPS / TOPICAL | 0.75 %w/v | ||
| EDETATE DISODIUM | EDETATE DISODIUM | 7FLD91C86K | LOTION / TOPICAL | 22 mg | ||
| POVIDONE | POVIDONE | FZ989GH94E | TABLET, FILM COATED, EXTENDED RELEASE / ORAL | 17 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | JELLY / NASAL | NA | ||
| SILICON DIOXIDE | SILICON DIOXIDE | ETJ7Z6XBU4 | SOLUTION / ORAL | 336 mg | ||
| SILICON DIOXIDE | SILICON DIOXIDE | ETJ7Z6XBU4 | POWDER, FOR SUSPENSION / ORAL | 2553 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | TABLET / ORAL | 42 mg | ||
| EDETATE DISODIUM | EDETATE DISODIUM | 7FLD91C86K | TABLET, DELAYED RELEASE / ORAL | 100 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | INJECTION / INTRACARDIAC | 70 mg | ||
| SILICON DIOXIDE | SILICON DIOXIDE | ETJ7Z6XBU4 | GEL / VAGINAL | 8 %w/w | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | SUSPENSION, EXTENDED RELEASE / ORAL | 40 mg | ||
| MAGNESIUM STEARATE | MAGNESIUM STEARATE | 70097M6I30 | GRANULE / ORAL | 629 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | INJECTION, POWDER, FOR SOLUTION / INTRAPLEURAL | 226 mg | ||
| STARCH, CORN | STARCH, CORN | O8232NY3SJ | TABLET, CHEWABLE / ORAL | 180 mg | ||
| POVIDONE | POVIDONE | FZ989GH94E | CAPSULE, DELAYED RELEASE PELLETS / ORAL | 32 mg | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | LIQUID / ORAL | 2 mg | ||
| EDETATE DISODIUM | EDETATE DISODIUM | 7FLD91C86K | LIQUID / INTRAVENOUS | 0.03 %w/v | ||
| EDETATE DISODIUM | EDETATE DISODIUM | 7FLD91C86K | SUSPENSION / ORAL | 30 mg | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | SWAB / TOPICAL | 34.6 %w/w | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | GRANULE, FOR SUSPENSION / ORAL | 80 mg | ||
| BENZALKONIUM CHLORIDE | BENZALKONIUM CHLORIDE | F5UM2KM3W7 | SPRAY / NASAL | 1 mg | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | FILM / BUCCAL | 0.22 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | POWDER, FOR SOLUTION / ORAL | NA | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | SOLUTION/ DROPS / AURICULAR (OTIC) | 18 mg | ||
| POVIDONE | POVIDONE | FZ989GH94E | SUSPENSION/ DROPS / OPHTHALMIC | 0.6 %w/v | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | SOLUTION, CONCENTRATE / ORAL | 2590 mg | ||
| BENZALKONIUM CHLORIDE | BENZALKONIUM CHLORIDE | F5UM2KM3W7 | SOLUTION / NASAL | 40.46 mg/100ml | ||
| POVIDONE | POVIDONE | FZ989GH94E | TABLET, EXTENDED RELEASE / ORAL | 101 mg | ||
| POVIDONE | POVIDONE | FZ989GH94E | SYSTEM / TOPICAL | 41 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | INJECTION / INFILTRATION | 648 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | SOLUTION / AURICULAR (OTIC) | 18 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | SOLUTION / SUBCUTANEOUS | 90 mg | ||
| HYPROMELLOSES | HYPROMELLOSE | 3NXW29V3WO | CAPSULE / ORAL | 1488 mg | ||
| TITANIUM DIOXIDE | TITANIUM DIOXIDE | 15FIX9V2JP | GUM, CHEWING / BUCCAL | 182 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE / ORAL | 530 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | JELLY / TOPICAL | NA | ||
| STEARIC ACID | STEARIC ACID | 4ELV7Z65AP | AEROSOL, FOAM / VAGINAL | 4 %w/w | ||
| SODIUM PHOSPHATE, MONOBASIC | SODIUM PHOSPHATE, MONOBASIC | 3980JIH2SW | INJECTION / INTRAMUSCULAR | 161 mg | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | SYRUP / ORAL | 81 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | PASTE / DENTAL | 20 %w/w | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | CAPSULE, DELAYED RELEASE / ORAL | 1.7 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | TABLET / ORAL | 231 mg | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | SOLUTION / ORAL | 100 mg | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | LOTION / TOPICAL | 351 mg | ||
| EDETATE DISODIUM | EDETATE DISODIUM | 7FLD91C86K | SUSPENSION/ DROPS / OPHTHALMIC | 1 mg | ||
| STARCH, CORN | STARCH, CORN | O8232NY3SJ | CAPSULE, DELAYED RELEASE / ORAL | 216 mg | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | AEROSOL / TOPICAL | 19.2 %w/w | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | SOLUTION / INTRAVENOUS | 0.02 %w/v | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | FILM, SOLUBLE / BUCCAL | 1 mg | ||
| PROPYLPARABEN | PROPYLPARABEN | Z8IX2SC1OH | ENEMA / RECTAL | 0.02 %w/w | ||
| SILICON DIOXIDE | SILICON DIOXIDE | ETJ7Z6XBU4 | POWDER / RESPIRATORY (INHALATION) | NA | ||
| PROPYLENE GLYCOL | PROPYLENE GLYCOL | 6DC9Q167V3 | INJECTION / INTRAMUSCULAR | 7459 mg | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | SOLUTION / OPHTHALMIC | 0.05 %w/w | ||
| SODIUM PHOSPHATE, MONOBASIC | SODIUM PHOSPHATE, MONOBASIC | 3980JIH2SW | SYSTEM / IONTOPHORESIS | 14.2 mg | ||
| SODIUM PHOSPHATE, MONOBASIC | SODIUM PHOSPHATE, MONOBASIC | 3980JIH2SW | INJECTION / INTRAVENOUS | 161 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | INJECTION, SOLUTION / INTRAVESICAL | 351 mg | ||
| CETYL ALCOHOL | CETYL ALCOHOL | 936JST6JCN | TABLET / ORAL | NA | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | SUSPENSION / ENDOTRACHEAL | 7.6 mg | ||
| SILICON DIOXIDE | SILICON DIOXIDE | ETJ7Z6XBU4 | TAMPON / VAGINAL | NA | ||
| METHYLPARABEN | METHYLPARABEN | A2I8C7HI9T | SOLUTION / INTRAVENOUS | 0.13 %w/v |
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A075010-001 | IBUPROFEN | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 |
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.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-09-14 22:38:34 | 2026-08 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 84e616aacf4f… | ||
| 2026-08-18 06:07:40 | 2026-07 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | caaa826d4ba7… | ||
| 2026-02-19 14:30 UTC | 2026-02 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 011fe1cb6892… | ||
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 31067a03dcf5… | ||
| 2025-08-23 18:47 UTC | 2025-08 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 6a471c1ec25d… | ||
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | fd3edfee7708… | ||
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | b8a1b40f171c… | ||
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 03ed91905a0d… | ||
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 2680178bc6a6… | ||
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 5bbf6a4d5a75… | ||
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | d8e5a09893c0… | ||
| 2024-10-29 15:01 UTC | 2024-10 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | d06236e962d9… | ||
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 79d66fd596c7… | ||
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 301d65b070ca… | ||
| 2024-06-18 03:08 UTC · 5 captures of this ZIP | 2024-06 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 1e350fbaab3a… | ||
| 2024-05-31 18:47 UTC | 2024-05 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 8072bd15b7f6… | ||
| 2022-06-29 02:47 UTC · 2 captures of this ZIP | 2022-06 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 5c6f7cd8ea54… | ||
| 2022-04-08 23:34 UTC | 2022-04 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 5d02ea3f76ae… | ||
| 2022-04-04 05:41 UTC | 2022-04 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 4b0b4de00fa7… | ||
| 2019-12-13 00:20 UTC | 2019-12 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 74a2ff9319b5… | ||
| 2022-03-09 01:35 UTC | 2022-03 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | bb7c543d1eb4… | ||
| 2021-12-28 21:50 UTC | 2021-12 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 782e0a99824c… | ||
| 2021-05-05 16:15 UTC · 3 captures of this ZIP | 2021-05 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 87673890dc5c… | ||
| 2021-03-12 10:30 UTC | 2021-03 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 5aa47cf7b7d7… | ||
| 2020-12-22 03:56 UTC | 2020-12 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 8869cabd3fbd… | ||
| 2020-11-12 02:37 UTC | 2020-11 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | c0c555d07b60… | ||
| 2019-12-14 00:12 UTC | 2019-12 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 3f01610625f2… | ||
| 2019-09-15 20:21 UTC | 2019-09 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | b00525d2431f… | ||
| 2019-07-19 19:46 UTC | 2019-07 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | ea99ee380514… | ||
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 6a51e52b5d6a… | ||
| 2024-02-18 07:12 UTC | 2024-02 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 1c564ffb4f44… | ||
| 2023-12-20 04:57 UTC | 2023-12 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | ea1830bbd6c7… | ||
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | a72a2bbeb626… | ||
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 9b2671bbb829… | ||
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | a67488948f0b… | ||
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 3f0d92c62455… | ||
| 2023-05-13 08:27 UTC | 2023-05 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 053a50430f4f… | ||
| 2023-01-26 05:58 UTC | 2023-01 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 3bdfa0b2c4d7… | ||
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | 3a93d1ddd44b… | ||
| 2022-10-28 04:53 UTC | 2022-10 | A075010-001 | IBUPROFEN | 200MG | TABLET / ORAL | 1999-03-01 | f41ea6bd6efb… |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| f1c6e667-8c30-4519-a961-98546c966463 | fa23be25-61c3-491c-b9e6-a5275c9bdc13 | 2011-05-04 | Warnings | f1c6e667-8c30-4519-a961-98546c966463 fa23be25-61c3-491c-b9e6-a5275c9bdc13 |
Adverse event summaries are temporarily unavailable. Other product information remains available.