| 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 |