Label: DIGESTIVE RELIEF- bismuth subsalicylate tablet, film coated
- NDC Code(s): 21130-125-40
- Packager: SAFEWAY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 14, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- 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: Contains salicylate. Do not take if you are
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- allergic to salicylates (including aspirin)
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- taking other salicylate products.
Ask a doctor or pharmacist before use if you are
taking any drug for
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- anticoagulation (thinning the blood)
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- diabetes
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- gout
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- arthritis
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Directions
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- swallow with water, do not chew
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- adults and children 12 years and older: 2 caplets every 1/2 to 1 hour as needed
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- do not exceed 8 doses (16 caplets) in 24 hours
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- use until diarrhea stops but not more than 2 days
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- children under 12 years: ask a doctor
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- drink plenty of clear fluids to help prevent dehydration caused by diarrhea
- Other Information
- Questions or comments?
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PRINCIPAL DISPLAY PANEL
NDC# 21130-125-40
Compare to the active ingredient Pepto-Bismol®*
Digestive Relief
Bismuth Subsalicylate 262 mg
Upset Stomach Reliever/ Antidiarrheal
5 Symptoms Digestive Relief
- •
- Heartburn
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- Indigestion
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- Nausea
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- Upset Stomach
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- Diarrhea
40 CAPLETS
TAMPER EVIDENT: DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING
Distributed by:
*This product is not manufactured or distributed by Procter & Gamble Inc., the distributor of Pepto-Bismol®.
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INGREDIENTS AND APPEARANCE
DIGESTIVE RELIEF
bismuth subsalicylate tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-125 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE 262 mg Inactive Ingredients Ingredient Name Strength CALCIUM CARBONATE (UNII: H0G9379FGK) CROSPOVIDONE (120 .MU.M) (UNII: 68401960MK) D&C RED NO. 27 (UNII: 2LRS185U6K) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM LAURYL SULFATE (UNII: 368GB5141J) Product Characteristics Color PINK Score no score Shape OVAL (Caplet) Size 16mm Flavor Imprint Code RP125 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-125-40 1 in 1 CARTON 10/05/2020 1 40 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 M008 10/05/2020 Labeler - SAFEWAY (009137209)