Easy Care First Aid Kit - Comprehensive

Manufacturer
Tender Corporation
Effective date
2017-03-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:12

Label at a glance#

ProductEasy Care First Aid Kit - Comprehensive
Active ingredientLIDOCAINE HYDROCHLORIDE, IBUPROFEN, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE, ACETAMINOPHEN, AMMONIA
Label structure38 sections

Indications and uses

Temporary relief of minor aches and pains associated with: common cold, headache, toothache, muscular aches, backache, arthritis, menstrual cramps, and reduction of fever

Dosage and administration

Adults and Children 2 years and older - dab directly on bite or sting, rub gently and reapply as needed Children under 2 years - ask a doctor

Label contents#

Full prescribing information#

Active Ingredients - After Bite Wipe

OTC - ACTIVE INGREDIENT SECTION

Ammonia 3.5%

Purpose - After Bite Wipe

OTC - PURPOSE SECTION

Counterirritant

Use - After Bite Wipe

INDICATIONS & USAGE SECTION

Temporarily protects and helps relieve minor skin irritation and itching due to - insect bites and stings, poison ivy, oak or sumac

Warnings - After Bite Wipes

WARNINGS SECTION

For External Use Only

Keep Out of Reach of Children - After Bite

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

Stop Use - After Bite Wipe

OTC - STOP USE SECTION

Stop use and ask a doctor if: Condition worsens, symptoms last more than 7 days or clear up and occur again within a few days

When Using - After Bite

OTC - WHEN USING SECTION

Do not get into eyes

Directions - After Bite Wipe

DOSAGE & ADMINISTRATION SECTION

Adults and Children 2 years and older - dab directly on bite or sting, rub gently and reapply as needed

Children under 2 years - ask a doctor

Active Ingredient - Aspirin

OTC - ACTIVE INGREDIENT SECTION

Aspirin (NSAID*) 325mg *nonsteroidal anti-inflammatory drug

Purpose - Aspirin

OTC - PURPOSE SECTION

Pain Reliever/Fever Reducer

When Using - Aspirin

OTC - WHEN USING SECTION

Reye's Syndrome: Children and teenagers who have or are recovering from chicken pox or 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 or 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 everyday while using this problem, take more for a longer time than directed.

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.

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

Stop use and Ask a Doctor if: you experience any of the following signs of stomach bleeding, you feel faint, vomit blood, have bloody or black stools, have stomach pain that does not get better, 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 painful areas, or any new symptoms appear.

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

Keep out of reach of Children. In case of overdose, get medical help or contact a poison control center right away.

Directions - Aspirin

DOSAGE & ADMINISTRATION SECTION

Do not use more than directed - the smallest effective dosage 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 as a doctor.

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

Avoid excessive heat and humidity, do not use any open or torn packets.

Use - Aspirin

INDICATIONS & USAGE SECTION

Temporariy relieves minor aches and pains associated with: headache, muscular aches, minor arthritis pain, backache, common cold, toothache, menstrual cramps, temorarily reduces fever.

Active Ingredient - Ibuprofen

OTC - ACTIVE INGREDIENT SECTION

Ibuprofen

Purpose - Ibuprofen

OTC - PURPOSE SECTION

Pain Reliever/Fever Reducer

Use - Ibuprofen

INDICATIONS & USAGE SECTION

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 and Precautions - Ibuprofen

WARNINGS SECTION

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, and 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.

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

Ask a doctor before use if stomach bleeding warning applies to you, you have had 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.

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.

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

Stop use and ask a doctor if you experience any of the following signs of stomach bleeding, feeling 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, redness or swelling is present in the painful area, any new symptoms appear.

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.

Keep out of reach of children. In case of overdose, get medical help or contact a poison control center right away.

Store at controlled room temperature, avoid excessive heat 40 degrees Celsius (104 degrees Fahrenheit); temper evident sealed packets, do not use any opened or torn packets.

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, 3 tablets may be use. Do not exceed 6 tablets in 24 hours, unless directed by a doctor. Children under 12 years: do not give children under 12 years of age.

Active Ingredient - APAP

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 500mg

Purpose - APAP

OTC - PURPOSE SECTION

Analgesic/antipyretic

Uses - APAP

INDICATIONS & USAGE SECTION

Temporary relief of minor aches and pains associated with: common cold, headache, toothache, muscular aches, backache, arthritis, menstrual cramps, and reduction of fever

Warnings and Precautions - APAP

WARNINGS SECTION

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 ever day while using this product.

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.

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 more than 10 days, fever gets worse or lasts 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 for children even if you do not notice any signs or symptoms. Do not exceed recommended dosage.

Store at 59-86 degrees F (15-30 degrees C), tamper evident sealed packets, do not use any open or torn packets.

Directions - APAP

OTC - WHEN USING SECTION

Adult and Children (12 years and older) take 2 tablets every 4 to 6 hours as needed. Do not take more than 12 tablets in 24 hours.

Children 6-11 years take 1 tablet every 4 to 6 hours as needed. Do not take more than 5 tablets in 24 hours.

Childen under 6 do not use this product

Active Ingredient - Diphenhydramine

OTC - ACTIVE INGREDIENT SECTION

Diphenhydramine Hydrochloride 25mg

Purpose - Diphenhydramine

OTC - PURPOSE SECTION

Antihistamine

Use - Diphenhydramine

INDICATIONS & USAGE SECTION

Temporarily relieves these symptoms due to hay fever or other respiratory allergies: runny nose, sneezing, itching nose or throat, itchy-watery eyes.

Temporarily relieves these symptoms due to the common cold: runny nose, sneezing

Warnings and Precautions - Diphenhydramine

WARNINGS SECTION

Do not use to make a child sleepy or with any other product containing diphenhydramine, even one that is used on skin.

Ask a doctor before use if you have: a breathing problem such as emphysema or chronic bronchitis, difficulty in urination due to enlargement of the prostate gland, or glaucoma.

Ask a doctor pharmacist before you use if you are taking sedatives or tranquilizers.

When using this product: marked drowsiness may occur, avoid alcoholic beverages, alcohol, sedatives and tranquilizers may increase the drowsiness effect, use caution when driving a motor vehicle or operating machinery, excitability may occur, especially in children.

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

Keep out of reach of Children. In case of overdose, contact a physician or poison control center immediately.

Each caplet may contain calcium 25mg. Store at room temperature 59-86 degrees F (15-30 C), protect from light and use by expiration date on packet. Tamper-evident sealed packets, do not use any opened or torn packets.

Directions - Diphenhydramine

DOSAGE & ADMINISTRATION SECTION

Do not use more than directed.

Adults and Children (12 Years and older) - take 1 to 2 caplets every 4 to 6 hours as needed. Do not take more than 12 caplets in 24 hours, or as directed by a doctor.

Do not give to children under 12 years of age.

Active Ingredients - After Cuts and Scrapes

OTC - ACTIVE INGREDIENT SECTION

Lidocaine Hydrochloride 2.5%

Benzalkonium Chloride .13%

Purpose - After Cuts and Scrapes

OTC - PURPOSE SECTION

Anesthetic

Antiseptic

Uses - After Cuts and Scrapes

INDICATIONS & USAGE SECTION

First aid for the temporary relief of pain and to protect from infection in minor cuts, scrapes and burns.

Warnings and Precautions - After Cuts and Scrapes

WARNINGS SECTION

For External Use Only.

When using this product: do not get into eyes, do not use in large quantities, particularly over raw surfaces or blistered areas.

Stop use and ask a doctor if rash, redness or swelling occurs or pain increases. In case of deep puncture wounds, animal bites or serious burns consult a doctor.

If swallowed, get medical help or contact a poison control center right away.

If in eyes, flush with water for 15 minutes and call a doctor.

Keep out of Reach of Children.

Directions - After Cuts and Scrapes

DOSAGE & ADMINISTRATION SECTION

Shake Well. Clean affected area. Spray on the area 1 to 3 times daily. Adults and children 2 years and older, apply to affected area. Children under 2 years, ask a doctor.

Active Ingredient - After Burn

OTC - ACTIVE INGREDIENT SECTION

Lidocaine Hydrochloride 2.5%

Purpose - After Burn

OTC - PURPOSE SECTION

Topical Analgesic

Use - After Burn

INDICATIONS & USAGE SECTION

For the temporary relief of pain due to minor burns, sunburn, minor cuts, scrapes or minor skin irritations

Warnings and Precautions - After Burn

WARNINGS SECTION

For external use only.

When using this product: avoid contact with eyes, do not use in large quantities, particularly over raw surfaces or blistered areas, do not use longer than 1 week unless directed by a doctor, or in case of deep puncture wounds, animal bites or serious burns, consult a doctor.

Stop use and ask a doctor if conditions or symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of Reach of Children.

If swallowed, get medical help or contact a poison control center right away.

If in eyes, flush with water for 15 minutes and call a doctor

Adults and Children 2 years and older, apply small amount to affected area, not more than 3 times daily.

Children under 2 years, consult a doctor.

Inactive Ingredients - After Burn

INACTIVE INGREDIENT SECTION

Aloe Vera Gel, Benzalkonium Chloride, Carbomer 980, glycerol, USP, herbal fragrance, menthol, polysorbate 20, Propylene glycol, purified water, sodium hydroxide (50%)

Package Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Comprehensive KitComprehensive KitAfter Cuts and ScrapesAfter Cuts and ScrapesAfter BurnAfter BurnAPAPAPAPAPAPAPAPAfter Bite WipeAfter Bite WipeAspirinAspirinAspirinAspirinIbuprofenIbuprofenIbuprofenIbuprofenDiphenhydramineDiphenhydramine

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198440acetaminophen 500 MG Oral TabletPSN1
212033aspirin 325 MG Oral TabletPSN1
1049630diphenhydrAMINE HCl 25 MG Oral TabletPSN1
310965ibuprofen 200 MG Oral TabletPSN1
1009433lidocaine HCl 2.5 % Topical GelPSN1
198440acetaminophen 500 MG Oral TabletSCD1
212033aspirin 325 MG Oral TabletSCD1
1049630diphenhydramine hydrochloride 25 MG Oral TabletSCD1
310965ibuprofen 200 MG Oral TabletSCD1
1009433lidocaine hydrochloride 0.025 MG/MG Topical GelSCD1
198440APAP 500 MG Oral TabletSY1
212033ASA 325 MG Oral TabletSY1
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY1
1009433lidocaine hydrochloride 2.5 % Topical GelSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ASPIRIN Pharmacologic Class Indexing3Indexing - Pharmacologic Class20191108
DIPHENHYDRAMINE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813
IBUPROFEN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20191108
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44224-2999-02020-01-31C16284748780-19d75b9cf-d2aa-f424-e053-dadaa90a57ceEasy Care Comprehensive First Aid Kit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44224-0001-2Easy Care First Aid Kit - Comprehensive0.7 mL in 1 PACKAGESWAB3 mL in .730 mg in 1mL1
44224-2999-0Easy Care First Aid Kit - Comprehensive1 in 1 BOXKIT11
44224-3300-0Easy Care First Aid Kit - Comprehensive30 mL in 1 BOTTLESOLUTION1 mL in 3026 mg in 1mL1
47682-097-99Easy Care First Aid Kit - Comprehensive2 in 1 PACKETTABLET, FILM COATED2325 mg1
47682-125-99Easy Care First Aid Kit - Comprehensive2 in 1 PACKETTABLET, FILM COATED2500 mg1
47682-184-46Easy Care First Aid Kit - Comprehensive1 in 1 PACKETTABLET, FILM COATED225 mg1
47682-700-99Easy Care First Aid Kit - Comprehensive2 in 1 PACKETTABLET, COATED2200 mg1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44224-0001EASY CARE FIRST AID KIT - COMPREHENSIVE (AMMONIA, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, ACETAMINOPHEN, LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Unmatched20170310_4a4e2759-49ef-20db-e054-00144ff8d46c.zip
44224-2999EASY CARE FIRST AID KIT - COMPREHENSIVE (AMMONIA, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, ACETAMINOPHEN, LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC, 7 package rows20170310_4a4e2759-49ef-20db-e054-00144ff8d46c.zip
44224-3300EASY CARE FIRST AID KIT - COMPREHENSIVE (AMMONIA, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, ACETAMINOPHEN, LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC20170310_4a4e2759-49ef-20db-e054-00144ff8d46c.zip
44224-5120EASY CARE FIRST AID KIT - COMPREHENSIVE (AMMONIA, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, ACETAMINOPHEN, LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC20170310_4a4e2759-49ef-20db-e054-00144ff8d46c.zip
47682-097EASY CARE FIRST AID KIT - COMPREHENSIVE (AMMONIA, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, ACETAMINOPHEN, LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC20170310_4a4e2759-49ef-20db-e054-00144ff8d46c.zip
47682-125EASY CARE FIRST AID KIT - COMPREHENSIVE (AMMONIA, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, ACETAMINOPHEN, LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC20170310_4a4e2759-49ef-20db-e054-00144ff8d46c.zip
47682-184EASY CARE FIRST AID KIT - COMPREHENSIVE (AMMONIA, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, ACETAMINOPHEN, LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC20170310_4a4e2759-49ef-20db-e054-00144ff8d46c.zip
47682-700EASY CARE FIRST AID KIT - COMPREHENSIVE (AMMONIA, ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, ACETAMINOPHEN, LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Current NDC, Legacy NDC20170310_4a4e2759-49ef-20db-e054-00144ff8d46c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
47682-184-47EA - Each47682-1849ad23d3d-85f4-4db3-893c-a0c41ee9487012017-05-03
47682-184-64EA - Each47682-184f555f4f0-8f4c-42b5-9a60-2a44dacb1dad12023-09-05

Products#

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

DailyMed product names page 1 of 2 · 54 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 58 matching rows.

Source Document#

Source XML

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 43.

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
A079174-001IBUPROFENIBUPROFEN200MGTABLET / ORAL2010-12-10

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 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-1084e616aacf4f…
2026-08-18 06:07:402026-07A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-1031067a03dcf5…
2025-08-23 18:47 UTC2025-08A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-106a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-1003ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-102680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-105bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-1079d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-101e350fbaab3a…
2024-05-31 18:47 UTC2024-05A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-108072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-105c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-105d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-104b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-1074a2ff9319b5…
2022-03-09 01:35 UTC2022-03A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-1087673890dc5c…
2021-03-12 10:30 UTC2021-03A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-105aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-108869cabd3fbd…
2020-11-12 02:37 UTC2020-11A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10c0c555d07b60…
2019-12-14 00:12 UTC2019-12A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-103f01610625f2…
2019-09-15 20:21 UTC2019-09A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10b00525d2431f…
2019-07-19 19:46 UTC2019-07A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-106a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-101c564ffb4f44…
2023-12-20 04:57 UTC2023-12A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-109b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-103f0d92c62455…
2023-05-13 08:27 UTC2023-05A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10053a50430f4f…
2023-01-26 05:58 UTC2023-01A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-103bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-103a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A079174-001IBUPROFEN200MGTABLET / ORAL2010-12-10f41ea6bd6efb…

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 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Medique IprinIBUPROFENUnifirst First Aid Corporation0607edb0-1b3a-2ccd-e054-00144ff8d46c2025-09-09WarningsExact identifier
ndc (package): 47682-700-99
ndc (product): 47682-700
ndc11 (package): 47682070099
Medique DiphenDIPHENHYDRAMINE HYDROCHLORIDEUnifirst First Aid Corporationb61ee2e0-2543-447d-9fc4-23363d46ce042025-09-08WarningsExact identifier
ndc (package): 47682-184-46
ndc (product): 47682-184
ndc11 (package): 47682018446
4a4e2759-49f0-20db-e054-00144ff8d46c4a4e2759-49ef-20db-e054-00144ff8d46c2017-03-09WarningsExact identifier
spl id: 4a4e2759-49f0-20db-e054-00144ff8d46c
spl set id: 4a4e2759-49ef-20db-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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