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Desitin Maximum Strength
Desitin Maximum Strength - 58232-0721-4 - (Zinc Oxide)
Drug Information of Desitin Maximum Strength
| Product NDC: | 58232-0721 |
| Proprietary Name: | Desitin Maximum Strength |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 400 mg/g & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desitin Maximum Strength
| Product NDC: | 58232-0721 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110908 |
Package Information of Desitin Maximum Strength
| Package NDC: | 58232-0721-4 |
| Package Description: | 1 TUBE in 1 CARTON (58232-0721-4) > 85 g in 1 TUBE |
NDC Information of Desitin Maximum Strength
| NDC Code | 58232-0721-4 |
| Proprietary Name | Desitin Maximum Strength |
| Package Description | 1 TUBE in 1 CARTON (58232-0721-4) > 85 g in 1 TUBE |
| Product NDC | 58232-0721 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110908 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 400 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
