Product NDC: | 49035-021 |
Proprietary Name: | BENZOYL PEROXIDE |
Non Proprietary Name: | BENZOYL PEROXIDE |
Active Ingredient(s): | & nbsp; BENZOYL PEROXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49035-021 |
Labeler Name: | Wal-Mart Stores Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100226 |
Package NDC: | 49035-021-13 |
Package Description: | 1 KIT in 1 KIT (49035-021-13) * 120 mL in 1 BOTTLE, PLASTIC * 60 mL in 1 BOTTLE, PLASTIC |
NDC Code | 49035-021-13 |
Proprietary Name | BENZOYL PEROXIDE |
Package Description | 1 KIT in 1 KIT (49035-021-13) * 120 mL in 1 BOTTLE, PLASTIC * 60 mL in 1 BOTTLE, PLASTIC |
Product NDC | 49035-021 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZOYL PEROXIDE |
Dosage Form Name | KIT |
Route Name | TOPICAL |
Start Marketing Date | 20100226 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Wal-Mart Stores Inc |
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