Product NDC: | 49580-3210 |
Proprietary Name: | Peptic Relief |
Non Proprietary Name: | Maximum Strength Pepto Bismol |
Active Ingredient(s): | 525 mg/15mL & nbsp; Maximum Strength Pepto Bismol |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49580-3210 |
Labeler Name: | Aaron Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090806 |
Package NDC: | 49580-3210-8 |
Package Description: | 237 mL in 1 BOTTLE, PLASTIC (49580-3210-8) |
NDC Code | 49580-3210-8 |
Proprietary Name | Peptic Relief |
Package Description | 237 mL in 1 BOTTLE, PLASTIC (49580-3210-8) |
Product NDC | 49580-3210 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Maximum Strength Pepto Bismol |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20090806 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Aaron Industries, Inc. |
Substance Name | BISMUTH SUBSALICYLATE |
Strength Number | 525 |
Strength Unit | mg/15mL |
Pharmaceutical Classes |