| 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 |