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zinc oxide
zinc oxide - 67777-226-03 - (zinc oxide)
Drug Information of zinc oxide
| Product NDC: | 67777-226 |
| Proprietary Name: | zinc oxide |
| Non Proprietary Name: | zinc oxide |
| Active Ingredient(s): | 1.8 g/100g & nbsp; zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of zinc oxide
| Product NDC: | 67777-226 |
| Labeler Name: | Dynarex Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110201 |
Package Information of zinc oxide
| Package NDC: | 67777-226-03 |
| Package Description: | 24 TUBE in 1 CASE (67777-226-03) > 114 g in 1 TUBE |
NDC Information of zinc oxide
| NDC Code | 67777-226-03 |
| Proprietary Name | zinc oxide |
| Package Description | 24 TUBE in 1 CASE (67777-226-03) > 114 g in 1 TUBE |
| Product NDC | 67777-226 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | zinc oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynarex Corporation |
| Substance Name | ZINC OXIDE |
| Strength Number | 1.8 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
