Label: PEPTO BISMOL DIARRHEA LIQUICAPS- bismuth subsalicylate capsule, liquid filled
- NDC Code(s): 37000-537-12, 37000-537-24, 37000-537-48
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 14, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each LiquiCap)
- 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
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Directions
• swallow with water, do not chew
• adults and children 12 years and over:
• 2 LiquiCaps every ½ hour or 4 LiquiCaps every 1 hour as needed
• do not exceed 16 LiquiCaps 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
- Questions?
- TAMPER EVIDENT: THIS PACKAGE IS SAFETY SEALED & CHILD RESISTANT. USE ONLY IF BLISTERS ARE INTACT. IF DIFFICULT TO OPEN, USE SCISSORS.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 48 LiquiCap Carton
-
INGREDIENTS AND APPEARANCE
PEPTO BISMOL DIARRHEA LIQUICAPS
bismuth subsalicylate capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-537 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 GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) SORBITOL (UNII: 506T60A25R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) GELATIN (UNII: 2G86QN327L) POVIDONE (UNII: FZ989GH94E) D&C RED NO. 33 (UNII: 9DBA0SBB0L) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) Product Characteristics Color pink Score no score Shape CAPSULE Size 14mm Flavor Imprint Code PB Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37000-537-12 1 in 1 CARTON 03/01/2019 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:37000-537-24 2 in 1 CARTON 03/01/2019 2 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:37000-537-48 4 in 1 CARTON 03/01/2019 3 12 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M008 03/01/2018 Labeler - The Procter & Gamble Manufacturing Company (004238200)