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Mustela 50 Sunscreen
Mustela 50 Sunscreen - 64768-2919-1 - (TITANIUM DIOXIDE and ZINC OXIDE)
Drug Information of Mustela 50 Sunscreen
| Product NDC: | 64768-2919 |
| Proprietary Name: | Mustela 50 Sunscreen |
| Non Proprietary Name: | TITANIUM DIOXIDE and ZINC OXIDE |
| Active Ingredient(s): | .852; .6674 g/14.2g; g/14.2g & nbsp; TITANIUM DIOXIDE and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mustela 50 Sunscreen
| Product NDC: | 64768-2919 |
| Labeler Name: | Expanscience Laboratories d/b/a Mustela |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130215 |
Package Information of Mustela 50 Sunscreen
| Package NDC: | 64768-2919-1 |
| Package Description: | 1 CONTAINER in 1 CARTON (64768-2919-1) > 14.2 g in 1 CONTAINER |
NDC Information of Mustela 50 Sunscreen
| NDC Code | 64768-2919-1 |
| Proprietary Name | Mustela 50 Sunscreen |
| Package Description | 1 CONTAINER in 1 CARTON (64768-2919-1) > 14.2 g in 1 CONTAINER |
| Product NDC | 64768-2919 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE and ZINC OXIDE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20130215 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Expanscience Laboratories d/b/a Mustela |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .852; .6674 |
| Strength Unit | g/14.2g; g/14.2g |
| Pharmaceutical Classes |
