Label: EQUATE BISMUTH STOMACH RELIEF CHEW- bismuth subsalicylate tablet, chewable
- NDC Code(s): 79903-219-24
- Packager: Walmart
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 7, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
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.
- DO NOT USE
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- OVERDOSAGE
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DOSAGE & ADMINISTRATION
Directions
- Fully chew before swallowing
- Adults and children 12 years and over:
- 2 chewable tablets every 1/2 hour or 4 chewable tablets every hour as needed for diarrhea.
- 2 chewable tablets every 1/2 hour to 1 hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea).
- Do not exceed 8 doses (16 chewable tablets) 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.
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INACTIVE INGREDIENT
Inactive ingredients: Beeswax, calcium carbonate, carmine, carnauba wax, citric acid, corn starch, corn syrup, dextrin, ethyl acetate, glycerin, FD&C red no. 40 aluminum lake, FD&C yellow no. 6 aluminum lake, gum arabic, hydrogenated coconut oil, maltodextrin, natural and artificial flavors, phosphoric acid, propylene glycol, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, vegetable oil (coconut and/or canola oil), water.
- OTHER SAFETY INFORMATION
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EQUATE BISMUTH STOMACH RELIEF CHEW
bismuth subsalicylate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-219 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE 262 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color pink Score no score Shape ROUND Size 14mm Flavor WINTERGREEN Imprint Code SR Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-219-24 24 in 1 BOTTLE; Type 0: Not a Combination Product 11/07/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M008 11/07/2023 Labeler - Walmart (051957769) Registrant - Bestco (002149136) Establishment Name Address ID/FEI Business Operations Bestco 002149136 manufacture(79903-219)