| Product NDC: | 0121-4803 |
| 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): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0121-4803 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090920 |
| Package NDC: | 0121-4803-30 |
| Package Description: | 4 TRAY in 1 CASE (0121-4803-30) > 10 CUP, UNIT-DOSE in 1 TRAY > 30 mL in 1 CUP, UNIT-DOSE |
| NDC Code | 0121-4803-30 |
| Proprietary Name | Pink Bismuth |
| Package Description | 4 TRAY in 1 CASE (0121-4803-30) > 10 CUP, UNIT-DOSE in 1 TRAY > 30 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 0121-4803 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth Subsalicylate |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20090920 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 262 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes |