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sunmark stomach relief - 49348-192-37 - (Bismuth subsalicylate)

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Drug Information of sunmark stomach relief

Product NDC: 49348-192
Proprietary Name: sunmark stomach relief
Non Proprietary Name: Bismuth subsalicylate
Active Ingredient(s): 262    mg/15mL & nbsp;   Bismuth subsalicylate
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark stomach relief

Product NDC: 49348-192
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part335
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20030821

Package Information of sunmark stomach relief

Package NDC: 49348-192-37
Package Description: 237 mL in 1 BOTTLE (49348-192-37)

NDC Information of sunmark stomach relief

NDC Code 49348-192-37
Proprietary Name sunmark stomach relief
Package Description 237 mL in 1 BOTTLE (49348-192-37)
Product NDC 49348-192
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bismuth subsalicylate
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20030821
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name BISMUTH SUBSALICYLATE
Strength Number 262
Strength Unit mg/15mL
Pharmaceutical Classes

Complete Information of sunmark stomach relief


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