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Pepto-Bismol and Pepto-Bismol - 37000-402-01 - (Bismuth Subsalicylate)

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Drug Information of Pepto-Bismol and Pepto-Bismol

Product NDC: 37000-402
Proprietary Name: Pepto-Bismol and Pepto-Bismol
Non Proprietary Name: Bismuth Subsalicylate
Active Ingredient(s):    & nbsp;   Bismuth Subsalicylate
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Pepto-Bismol and Pepto-Bismol

Product NDC: 37000-402
Labeler Name: Procter & Gamble Manufacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part335
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110912

Package Information of Pepto-Bismol and Pepto-Bismol

Package NDC: 37000-402-01
Package Description: 1 KIT in 1 PACKAGE (37000-402-01) * 473 mL in 1 BOTTLE, PLASTIC (37000-032-04) * 8 CELLO PACK in 1 CARTON (37000-477-10) > 6 TABLET in 1 CELLO PACK

NDC Information of Pepto-Bismol and Pepto-Bismol

NDC Code 37000-402-01
Proprietary Name Pepto-Bismol and Pepto-Bismol
Package Description 1 KIT in 1 PACKAGE (37000-402-01) * 473 mL in 1 BOTTLE, PLASTIC (37000-032-04) * 8 CELLO PACK in 1 CARTON (37000-477-10) > 6 TABLET in 1 CELLO PACK
Product NDC 37000-402
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bismuth Subsalicylate
Dosage Form Name KIT
Route Name
Start Marketing Date 20110912
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Procter & Gamble Manufacturing Company
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Pepto-Bismol and Pepto-Bismol


General Information