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Pepto-Bismol
Pepto-Bismol - 37000-019-02 - (Bismuth subsalicylate)
Drug Information of Pepto-Bismol
| Product NDC: | 37000-019 |
| Proprietary Name: | Pepto-Bismol |
| Non Proprietary Name: | Bismuth subsalicylate |
| Active Ingredient(s): | 1050 mg/30mL & nbsp; Bismuth subsalicylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pepto-Bismol
| Product NDC: | 37000-019 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19890331 |
Package Information of Pepto-Bismol
| Package NDC: | 37000-019-02 |
| Package Description: | 236 mL in 1 BOTTLE, PLASTIC (37000-019-02) |
NDC Information of Pepto-Bismol
| NDC Code | 37000-019-02 |
| Proprietary Name | Pepto-Bismol |
| Package Description | 236 mL in 1 BOTTLE, PLASTIC (37000-019-02) |
| Product NDC | 37000-019 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth subsalicylate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19890331 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 1050 |
| Strength Unit | mg/30mL |
| Pharmaceutical Classes |
