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ZINC OXIDE
ZINC OXIDE - 0168-0062-02 - (ZINC OXIDE)
Drug Information of ZINC OXIDE
| Product NDC: | 0168-0062 |
| Proprietary Name: | ZINC OXIDE |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 200 mg/g & nbsp; ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZINC OXIDE
| Product NDC: | 0168-0062 |
| Labeler Name: | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19680101 |
Package Information of ZINC OXIDE
| Package NDC: | 0168-0062-02 |
| Package Description: | 1 TUBE in 1 CARTON (0168-0062-02) > 56.7 g in 1 TUBE |
NDC Information of ZINC OXIDE
| NDC Code | 0168-0062-02 |
| Proprietary Name | ZINC OXIDE |
| Package Description | 1 TUBE in 1 CARTON (0168-0062-02) > 56.7 g in 1 TUBE |
| Product NDC | 0168-0062 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19680101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 200 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
