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SUNSCREEN
SUNSCREEN - 43239-201-13 - (ZINC OXIDE)
Drug Information of SUNSCREEN
| Product NDC: | 43239-201 |
| Proprietary Name: | SUNSCREEN |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 20 g/100g & nbsp; ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNSCREEN
| Product NDC: | 43239-201 |
| Labeler Name: | ERBAVIVA INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120710 |
Package Information of SUNSCREEN
| Package NDC: | 43239-201-13 |
| Package Description: | 75 g in 1 TUBE (43239-201-13) |
NDC Information of SUNSCREEN
| NDC Code | 43239-201-13 |
| Proprietary Name | SUNSCREEN |
| Package Description | 75 g in 1 TUBE (43239-201-13) |
| Product NDC | 43239-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120710 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ERBAVIVA INC. |
| Substance Name | ZINC OXIDE |
| Strength Number | 20 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
