Product NDC: | 41250-551 |
Proprietary Name: | Medicated Body Powder |
Non Proprietary Name: | MENTHOL |
Active Ingredient(s): | .15; 1 kg/100kg; kg/100kg & nbsp; MENTHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41250-551 |
Labeler Name: | Meijer Distribution, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090505 |
Package NDC: | 41250-551-38 |
Package Description: | .283 kg in 1 BOTTLE, PUMP (41250-551-38) |
NDC Code | 41250-551-38 |
Proprietary Name | Medicated Body Powder |
Package Description | .283 kg in 1 BOTTLE, PUMP (41250-551-38) |
Product NDC | 41250-551 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MENTHOL |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20090505 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Meijer Distribution, Inc |
Substance Name | MENTHOL; ZINC OXIDE |
Strength Number | .15; 1 |
Strength Unit | kg/100kg; kg/100kg |
Pharmaceutical Classes |