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Zinc Oxide
Zinc Oxide - 42213-365-48 - (Zinc Oxide)
Drug Information of Zinc Oxide
| Product NDC: | 42213-365 |
| 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: | 42213-365 |
| Labeler Name: | Ultra Seal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120503 |
Package Information of Zinc Oxide
| Package NDC: | 42213-365-48 |
| Package Description: | 1 TUBE in 1 CARTON (42213-365-48) > 56 g in 1 TUBE (42213-365-56) |
NDC Information of Zinc Oxide
| NDC Code | 42213-365-48 |
| Proprietary Name | Zinc Oxide |
| Package Description | 1 TUBE in 1 CARTON (42213-365-48) > 56 g in 1 TUBE (42213-365-56) |
| Product NDC | 42213-365 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120503 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ultra Seal Corporation |
| Substance Name | ZINC OXIDE |
| Strength Number | 200 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
