Label: KAOPECTATE PEPPERMINT FLAVOR ANTI DIARRHEAL- bismuth subsalicylate liquid
- NDC Code(s): 55505-199-36, 55505-199-64
- Packager: Kramer Laboratories
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 15, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- Warnings
-
SPL UNCLASSIFIED SECTION
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.
Ask a doctor or pharmacist before use if you are taking any drug for
- diabetes
- gout
- arthritis
- anticoagulation (thinning the blood)
- diabetes
-
Directions
- shake well immediately before each use
- only use pre-measured dose cup
- adults and children 12 years of age and older:
- 1 dose (30 mL) every 1/2 hour to 1 hour as needed.
- do not exceed 8 doses (240 mL) 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 Ingredients
-
Principal Display Panel
NEW IMPROVED TASTE!
Kaopectate®
Bismuth Subsalicylate 262 MG
• Anti-Diarrheal • Upset Stomach Reliever
Diarrhea &
Upset Stomach
✓ Begins controlling symptoms from the first dose
✓ Quickly relieves urgency, gas, and cramping
✓ Effective on diarrhea from bacteria,
viruses, and other causes
11 fl oz (325mL)
Peppermint Flavor
681PPT11KA0 FKaopectate Peppermint 11 oz
Do not use if inner seal is broken
or missing
Kramer Laboratories
Bridgewater, NJ 08807
1-800-824-4894
Lot:
Exp:
PEEL CORNER TO READ COMPLETE
DRUG FACTS AND INFORMATION
681PPT11KA0LB
-
INGREDIENTS AND APPEARANCE
KAOPECTATE PEPPERMINT FLAVOR ANTI DIARRHEAL
bismuth subsalicylate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55505-199 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 in 15 mL Inactive Ingredients Ingredient Name Strength Carboxymethylcellulose Sodium, Unspecified (UNII: K679OBS311) Fd&C Red No. 40 (UNII: WZB9127XOA) Microcrystalline Cellulose (UNII: OP1R32D61U) SODIUM SALICYLATE (UNII: WIQ1H85SYP) SORBIC ACID (UNII: X045WJ989B) SUCROSE (UNII: C151H8M554) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color Score Shape Size Flavor PEPPERMINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55505-199-36 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 2 NDC:55505-199-64 325 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M008 10/01/2020 Labeler - Kramer Laboratories (122720675)