Product NDC: | 67777-234 |
Proprietary Name: | Menthol and Zinc Oxide |
Non Proprietary Name: | Menthol and Zinc Oxide |
Active Ingredient(s): | .44; 21 g/100g; g/100g & nbsp; Menthol and Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67777-234 |
Labeler Name: | Dynarex Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100511 |
Package NDC: | 67777-234-01 |
Package Description: | 2 BOX in 1 CASE (67777-234-01) > 144 POUCH in 1 BOX > 3.5 g in 1 POUCH |
NDC Code | 67777-234-01 |
Proprietary Name | Menthol and Zinc Oxide |
Package Description | 2 BOX in 1 CASE (67777-234-01) > 144 POUCH in 1 BOX > 3.5 g in 1 POUCH |
Product NDC | 67777-234 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Menthol and Zinc Oxide |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20100511 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Dynarex Corporation |
Substance Name | MENTHOL; ZINC OXIDE |
Strength Number | .44; 21 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |