Label: ASPIRIN tablet
- NDC Code(s): 57896-901-01, 57896-901-10, 57896-901-27
- Packager: Geri-Care Pharmaceuticals, Corp
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 8, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
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:
- facial swelling
- shock
- hives
- asthma (wheezing)
Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you
- are age 60 or older
- 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
- have had stomach ulcers or bleeding problems
- take a blood thinning (anticoagulant) or steroid drug
Do not use
- if you are allergic to aspirin or any other pain reliever/fever reducer
- if you have ever had an allergic reaction to this product or any of its ingredients
Ask a doctor before use if
- you have asthma
- 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
taking a prescription drug for
- gout
- diabetes
- arthritis
Stop use and ask a doctor if
- an allergic reaction occurs. Seek medical help right away.
- you experience any of the following signs of stomach bleeding:
- vomit blood
- have bloody or black stools
- have stomach pain that does not get better
- feel faint
- ringing in the ears or a loss of hearing occurs
- pain gets worse or lasts more than 10 days
- fever gets worse or lasts more than 3 days
- redness or swelling is present
- new symptoms occur
These could be signs of a serious condition.
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Directions
- do not take more than directed
- drink a full glass of water with each dose
- adults and children 12 years and over: take 1 or 2 tablets every 4 hours or 3 tablets every 6 hours not to exceed 12 tablets in 24 hours unless directed by a doctor
- children under 12 years: do not use unless directed by a doctor
- Other information
- Inactive ingredient
- Questions or comments?
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Principal Display Panel
NDC 57896-901-01
GERI CARE®
ASPIRIN
325 mg (NSAID)PAIN RELIEVER / FEVER REDUCER
REGULAR STRENGTH
Compare to active ingredient
in BAYER® Aspirin **100 TABLETS
Actual Size
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSING**This product is not manufactured or distributed by Bayer AG, owner
of the registered trademark Bayer® Aspirin.50844
REV0122D24912DISTRIBUTED BY: GERI-CARE PHARMACEUTICAL CORP.
1295 Towbin Ave., Lakewood, NJ 08701
Geri Care 44-249
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INGREDIENTS AND APPEARANCE
ASPIRIN
aspirin tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57896-901 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 325 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color white Score no score Shape ROUND Size 10mm Flavor Imprint Code 44;249;ASPIRIN Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57896-901-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 08/04/1993 2 NDC:57896-901-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 08/04/1993 3 NDC:57896-901-27 250 in 1 BOTTLE; Type 0: Not a Combination Product 08/04/1993 08/28/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 08/04/1993 Labeler - Geri-Care Pharmaceuticals, Corp (611196254) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(57896-901) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(57896-901) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(57896-901)