| Product NDC: | 29500-9091 |
| Proprietary Name: | Personal Care |
| Non Proprietary Name: | Medicated Foot Powder |
| Active Ingredient(s): | 20 mg/2g & nbsp; Medicated Foot Powder |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 29500-9091 |
| Labeler Name: | Personal Care Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090901 |
| Package NDC: | 29500-9091-1 |
| Package Description: | 283 g in 1 BOTTLE (29500-9091-1) |
| NDC Code | 29500-9091-1 |
| Proprietary Name | Personal Care |
| Package Description | 283 g in 1 BOTTLE (29500-9091-1) |
| Product NDC | 29500-9091 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Medicated Foot Powder |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Personal Care Products, Inc. |
| Substance Name | MENTHOL |
| Strength Number | 20 |
| Strength Unit | mg/2g |
| Pharmaceutical Classes |