| Product NDC: | 0536-5700 |
| Proprietary Name: | Rugby 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) |
| Product NDC: | 0536-5700 |
| Labeler Name: | Rugby Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040323 |
| Package NDC: | 0536-5700-98 |
| Package Description: | 454 g in 1 JAR (0536-5700-98) |
| NDC Code | 0536-5700-98 |
| Proprietary Name | Rugby Zinc Oxide |
| Package Description | 454 g in 1 JAR (0536-5700-98) |
| Product NDC | 0536-5700 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20040323 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rugby Laboratories |
| Substance Name | ZINC OXIDE |
| Strength Number | 200 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |