| Product NDC: | 0536-1810 |
| Proprietary Name: | PINK BISMUTH |
| 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) |
| Product NDC: | 0536-1810 |
| Labeler Name: | Rugby Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120401 |
| Package NDC: | 0536-1810-59 |
| Package Description: | 237 mL in 1 BOTTLE (0536-1810-59) |
| NDC Code | 0536-1810-59 |
| Proprietary Name | PINK BISMUTH |
| Package Description | 237 mL in 1 BOTTLE (0536-1810-59) |
| Product NDC | 0536-1810 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | bismuth subsalicylate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rugby Laboratories, Inc. |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 262 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes |