Label: ASPIRIN ENTERIC COATED- aspirin tablet, delayed release
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NDC Code(s):
59779-600-06,
59779-600-07,
59779-600-14,
59779-600-16, view more59779-600-17, 59779-600-27, 59779-600-29, 59779-600-32, 59779-600-90, 59779-600-91, 59779-600-99
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 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 other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others]
- are age 60 or older
- take more or for a longer time than directed
- have had stomach ulcers or bleeding problems
- have 3 or more alcoholic drinks every day while using this product
- 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
- 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 have asthma
- 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
- feel faint
- have bloody or black stools
- 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
♥CVS
Health®Compare to the active ingredient
in Bayer® Low Dose Aspirin†Coated Tablets
Low Dose
Aspirin
Pain Reliever (NSAID)• Safety Coated
• Aspirin Regimen§81
mg§Talk to your doctor
or other healthcare
provider before
using this product
for your heart.Actual
Size500 ENTERIC COATED TABLETS
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® Low Dose Aspirin. 50844 REV0122C60014Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2022 CVS/pharmacy
CVS.com®
1-800-SHOP CVS
V-11112100% money back
guaranteed.
CVS.com/returnpolicyCVS 44-600A
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INGREDIENTS AND APPEARANCE
ASPIRIN ENTERIC COATED
aspirin tablet, delayed releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-600 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 STARCH, CORN (UNII: O8232NY3SJ) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) 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) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) 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 yellow 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:59779-600-27 1 in 1 CARTON 05/01/2011 1 32 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:59779-600-32 1 in 1 CARTON 05/01/2011 2 120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:59779-600-06 1 in 1 CARTON 05/01/2011 3 200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:59779-600-17 300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2011 5 NDC:59779-600-14 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2011 6 NDC:59779-600-16 1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2011 7 NDC:59779-600-07 1 in 1 CARTON 05/01/2011 10/19/2017 7 36 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 8 NDC:59779-600-99 2 in 1 CARTON 05/01/2011 10/19/2017 8 120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 9 NDC:59779-600-29 1 in 1 CARTON 05/01/2011 10/19/2017 9 150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10 NDC:59779-600-90 1 in 1 CARTON 05/01/2011 07/13/2022 10 230 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11 NDC:59779-600-91 360 in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2011 07/13/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 05/01/2011 Labeler - CVS Pharmacy (062312574) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(59779-600) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(59779-600) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(59779-600) , pack(59779-600) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(59779-600)