Label: BISMUTH SUBSALICYLATE tablet, film coated
- NDC Code(s): 69842-346-12, 69842-346-28
- Packager: CVS Pharmacy, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 23, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- PURPOSE
- Uses
-
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
- allergic to salicylates (including aspirin)
- taking other salicylate products.
Ask a doctor or pharmacist before use if you are
taking any drug for
- anticoagulation (thinning the blood)
- diabetes
- gout
- arthritis
-
Directions
- swallow caplets with water, do not chew
- adults and children 12 years and over: 2 caplets (1 dose) every 1/2 to 4 cpalets (2 doses) every hour as needed for diarrhea
- 2 cpaltes (1 dose) every 1/2 hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea)
- do not exceed 8 doses (16 caplets) in 24 hours
- use until diarrhea stops but not more than 2 days
- children under 12 years: ask a doctor
- drink plenty of clear fluids to help prevent dehydration caused by diarrhea
- Other Information
- INACTIVE INGREDIENT
- Questions or comments?
-
SPL UNCLASSIFIED SECTION
RETAIN CARTON FOR FULL LABELING INFORMATION
*This product is not manufactured or distributed by Procter & Gamble Company, the owner of registered trademark Pepto-Bismol®.
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2024 CVS/pharmacy
CVS.com® 1-800-SHOP CVS
V-30287
Product of Mexico. Manufactured and packaged in U.S.A. using domestic and improted ingredients.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BISMUTH SUBSALICYLATE
bismuth subsalicylate tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-346 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 MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TRIACETIN (UNII: XHX3C3X673) LIGHT MINERAL OIL (UNII: N6K5787QVP) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) CROSPOVIDONE (UNII: 2S7830E561) HYPROMELLOSES (UNII: 3NXW29V3WO) POVIDONE K30 (UNII: U725QWY32X) SODIUM LAURYL SULFATE (UNII: 368GB5141J) STEARIC ACID (UNII: 4ELV7Z65AP) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white Score no score Shape OVAL Size 17mm Flavor Imprint Code V Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-346-28 1 in 1 CARTON 07/06/2018 1 40 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:69842-346-12 1 in 1 CARTON 07/06/2018 2 24 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 M001 07/06/2018 Labeler - CVS Pharmacy, Inc. (062312574)