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Menthol and Zinc Oxide
Menthol and Zinc Oxide - 67777-234-03 - (Menthol and Zinc Oxide)
Drug Information of Menthol and Zinc Oxide
| 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) |
Labeler Information of Menthol and Zinc Oxide
| 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 Information of Menthol and Zinc Oxide
| Package NDC: | 67777-234-03 |
| Package Description: | 24 TUBE in 1 CASE (67777-234-03) > 113 g in 1 TUBE |
NDC Information of Menthol and Zinc Oxide
| NDC Code | 67777-234-03 |
| Proprietary Name | Menthol and Zinc Oxide |
| Package Description | 24 TUBE in 1 CASE (67777-234-03) > 113 g in 1 TUBE |
| 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 |
