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ZINC OXIDE
ZINC OXIDE - 11822-0081-3 - (ZINC OXIDE)
Drug Information of ZINC OXIDE
| Product NDC: | 11822-0081 |
| 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: | 11822-0081 |
| Labeler Name: | RiteAid |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090519 |
Package Information of ZINC OXIDE
| Package NDC: | 11822-0081-3 |
| Package Description: | 57 g in 1 TUBE (11822-0081-3) |
NDC Information of ZINC OXIDE
| NDC Code | 11822-0081-3 |
| Proprietary Name | ZINC OXIDE |
| Package Description | 57 g in 1 TUBE (11822-0081-3) |
| Product NDC | 11822-0081 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20090519 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | RiteAid |
| Substance Name | ZINC OXIDE |
| Strength Number | 200 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
