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Mustela
Mustela - 64768-2918-1 - (Zinc Oxide)
Drug Information of Mustela
| Product NDC: | 64768-2918 |
| Proprietary Name: | Mustela |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 8.3 g/83g & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mustela
| Product NDC: | 64768-2918 |
| Labeler Name: | Expanscience Laboratoires d/b/a Mustela |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100719 |
Package Information of Mustela
| Package NDC: | 64768-2918-1 |
| Package Description: | 1 TUBE in 1 CARTON (64768-2918-1) > 55 g in 1 TUBE |
NDC Information of Mustela
| NDC Code | 64768-2918-1 |
| Proprietary Name | Mustela |
| Package Description | 1 TUBE in 1 CARTON (64768-2918-1) > 55 g in 1 TUBE |
| Product NDC | 64768-2918 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100719 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Expanscience Laboratoires d/b/a Mustela |
| Substance Name | ZINC OXIDE |
| Strength Number | 8.3 |
| Strength Unit | g/83g |
| Pharmaceutical Classes |
