Product NDC: | 49348-834 |
Proprietary Name: | Medicated Body |
Non Proprietary Name: | MENTHOL, ZINC OXIDE |
Active Ingredient(s): | .15; 1 g/100kg; g/100kg & nbsp; MENTHOL, ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49348-834 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19940618 |
Package NDC: | 49348-834-92 |
Package Description: | .283 kg in 1 BOTTLE, PLASTIC (49348-834-92) |
NDC Code | 49348-834-92 |
Proprietary Name | Medicated Body |
Package Description | .283 kg in 1 BOTTLE, PLASTIC (49348-834-92) |
Product NDC | 49348-834 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MENTHOL, ZINC OXIDE |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 19940618 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | McKesson |
Substance Name | MENTHOL; ZINC OXIDE |
Strength Number | .15; 1 |
Strength Unit | g/100kg; g/100kg |
Pharmaceutical Classes |