Label: ASPIRIN ENTERIC COATED LOW DOSE- aspirin tablet, delayed release
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NDC Code(s):
0363-6450-07,
0363-6450-12,
0363-6450-14,
0363-6450-32, view more0363-6450-60
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 24, 2024
If you are a consumer or patient please visit this version.
- 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:
- hives
- facial swelling
- shock
- asthma (wheezing)
Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you
- take more or for a longer time than directed
- take a blood thinning (anticoagulant) or steroid drug
- have had stomach ulcers or bleeding problems
- have 3 or more alcoholic drinks every day while using this product
- are age 60 or older
- take other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others]
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
- stomach bleeding warning applies to you
- you have a history of stomach problems, such as heartburn
- you are taking a diuretic
- you have high blood pressure, heart disease, liver cirrhosis, or kidney disease
- you have asthma
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:
- have bloody or black stools
- feel faint
- vomit blood
- have stomach pain that does not get better
- 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.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
VALUE SIZE NDC 0363-6450-14
Walgreens
Compare to the active ingredient in
St. Joseph® Low Dose 81 mg Aspirin††EASY-OPEN
Aspirin 81
81 mg / PAIN RELIEVER (NSAID)Low Dose
Enteric-Coated500
TABLETSACTUAL SIZE
HEART
HEALTH****Talk to your doctor or other healthcare provider before using this product for your heart.
NOT FOR HOUSEHOLDS WITH YOUNG CHILDREN
TAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSING††This product is not manufactured or distributed by Foundation
Consumer Healthcare, LLC, owner of the registered
trademark St. Joseph® Low Dose 81 mg Aspirin.50844 ORG012264514
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com ©2021 Walgreen Co.Walgreens 44-645
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INGREDIENTS AND APPEARANCE
ASPIRIN ENTERIC COATED LOW DOSE
aspirin tablet, delayed releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-6450 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 81 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, CORN (UNII: O8232NY3SJ) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) METHACRYLIC ACID (UNII: 1CS02G8656) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYDEXTROSE (UNII: VH2XOU12IE) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) SHELLAC (UNII: 46N107B71O) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) SODIUM BICARBONATE (UNII: 8MDF5V39QO) SODIUM LAURYL SULFATE (UNII: 368GB5141J) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIACETIN (UNII: XHX3C3X673) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) Product Characteristics Color pink Score no score Shape ROUND Size 6mm Flavor Imprint Code L Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-6450-14 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/25/2014 2 NDC:0363-6450-07 1 in 1 CARTON 07/25/2014 07/08/2018 2 36 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:0363-6450-12 1 in 1 CARTON 07/25/2014 09/21/2017 3 100 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:0363-6450-60 1 in 1 CARTON 07/25/2014 04/27/2022 4 180 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:0363-6450-32 1 in 1 CARTON 07/25/2014 04/22/2023 5 120 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 07/25/2014 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(0363-6450) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(0363-6450) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(0363-6450) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(0363-6450) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(0363-6450) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(0363-6450)