Product NDC: | 0363-0551 |
Proprietary Name: | Body |
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: | 0363-0551 |
Labeler Name: | Walgreen Co. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20030731 |
Package NDC: | 0363-0551-38 |
Package Description: | 283 g in 1 BOTTLE (0363-0551-38) |
NDC Code | 0363-0551-38 |
Proprietary Name | Body |
Package Description | 283 g in 1 BOTTLE (0363-0551-38) |
Product NDC | 0363-0551 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Menthol, zinc oxide |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20030731 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Walgreen Co. |
Substance Name | MENTHOL; ZINC OXIDE |
Strength Number | 1.5; 10 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |