Label: PAIN RELIEF ASPIRIN LOW DOSE- aspirin tablet, delayed release
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NDC Code(s):
11822-0600-2,
11822-0600-3,
11822-0600-4,
11822-0600-6, view more11822-0600-7
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 8, 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
- are age 60 or older
- have had stomach ulcers or bleeding problems
- take a blood thinning (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
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
- have bloody or black stools
- feel faint
- 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
Compare to the active ingredient in
Bayer® Low Dose Aspirin**NDC 11822-0600-7
Talk to your doctor or other healthcare
provider before using this product for
your heart.LOW DOSE PAIN RELIEF
ASPIRIN
ASPIRIN 81 mg
PAIN RELIEVER (NSAID)Aspirin regimen
Safety coatedACTUAL
SIZE300
ENTERIC
COATED TABLETSNOT FOR
HOUSEHOLDS
WITH YOUNG
CHILDRENTAMPER 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 REV0122B60017DISTRIBUTED BY: RITE AID, 200 NEWBERRY COMMONS, ETTERS, PA 17319 www.riteaid.com
SATISFACTION GUARANTEE: If you’re not satisfied, we’ll happily refund your money.
Rite Aid 44-600A
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INGREDIENTS AND APPEARANCE
PAIN RELIEF ASPIRIN LOW DOSE
aspirin tablet, delayed releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0600 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:11822-0600-2 1 in 1 CARTON 03/01/2023 1 32 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:11822-0600-3 1 in 1 CARTON 02/12/2008 2 120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:11822-0600-6 1 in 1 CARTON 02/12/2008 3 200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:11822-0600-7 300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/12/2008 5 NDC:11822-0600-4 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/12/2008 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 02/12/2008 Labeler - Rite Aid Corporation (014578892) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(11822-0600) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(11822-0600) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(11822-0600) , pack(11822-0600) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(11822-0600)