Product NDC: | 56062-302 |
Proprietary Name: | original formula |
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: | 56062-302 |
Labeler Name: | Publix Super Markets Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part335 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19950329 |
Package NDC: | 56062-302-34 |
Package Description: | 237 mL in 1 BOTTLE (56062-302-34) |
NDC Code | 56062-302-34 |
Proprietary Name | original formula |
Package Description | 237 mL in 1 BOTTLE (56062-302-34) |
Product NDC | 56062-302 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Bismuth subsalicylate |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19950329 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Publix Super Markets Inc |
Substance Name | BISMUTH SUBSALICYLATE |
Strength Number | 262 |
Strength Unit | mg/15mL |
Pharmaceutical Classes |