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