| Product NDC: | 58232-0719 |
| Proprietary Name: | Desitin Rapid Relief Creamy |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 132.1 mg/g & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58232-0719 |
| 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 FINAL |
| Start Marketing Date: | 20100601 |
| Package NDC: | 58232-0719-6 |
| Package Description: | 454 g in 1 JAR (58232-0719-6) |
| NDC Code | 58232-0719-6 |
| Proprietary Name | Desitin Rapid Relief Creamy |
| Package Description | 454 g in 1 JAR (58232-0719-6) |
| Product NDC | 58232-0719 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 132.1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |