| Product NDC: | 0869-0551 |
| Proprietary Name: | Medicated |
| Non Proprietary Name: | menthol, zinc oxide |
| Active Ingredient(s): | 1.5; 10 mg/g; mg/g & nbsp; menthol, zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0869-0551 |
| Labeler Name: | Vi-Jon |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20030812 |
| Package NDC: | 0869-0551-38 |
| Package Description: | 283 g in 1 BOTTLE, DISPENSING (0869-0551-38) |
| NDC Code | 0869-0551-38 |
| Proprietary Name | Medicated |
| Package Description | 283 g in 1 BOTTLE, DISPENSING (0869-0551-38) |
| Product NDC | 0869-0551 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | menthol, zinc oxide |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20030812 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Vi-Jon |
| Substance Name | MENTHOL; ZINC OXIDE |
| Strength Number | 1.5; 10 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |