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Zinc Oxide
Zinc Oxide - 67777-222-01 - (Zinc Oxide)
Drug Information of Zinc Oxide
| Product NDC: | 67777-222 |
| 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: | 67777-222 |
| Labeler Name: | Dynarex Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100316 |
Package Information of Zinc Oxide
| Package NDC: | 67777-222-01 |
| Package Description: | 72 TUBE in 1 CASE (67777-222-01) > 56.68 g in 1 TUBE |
NDC Information of Zinc Oxide
| NDC Code | 67777-222-01 |
| Proprietary Name | Zinc Oxide |
| Package Description | 72 TUBE in 1 CASE (67777-222-01) > 56.68 g in 1 TUBE |
| Product NDC | 67777-222 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100316 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynarex Corporation |
| Substance Name | ZINC OXIDE |
| Strength Number | 200 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
