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SUNSCREEN
SUNSCREEN - 66538-101-12 - (OCTINOXATE ZINC OXIDE)
Drug Information of SUNSCREEN
| Product NDC: | 66538-101 |
| Proprietary Name: | SUNSCREEN |
| Non Proprietary Name: | OCTINOXATE ZINC OXIDE |
| Active Ingredient(s): | 7.5; 6 g/100g; g/100g & nbsp; OCTINOXATE ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNSCREEN
| Product NDC: | 66538-101 |
| Labeler Name: | COSMOCEUTICAL RESEARCH CENTER INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111128 |
Package Information of SUNSCREEN
| Package NDC: | 66538-101-12 |
| Package Description: | 50 g in 1 JAR (66538-101-12) |
NDC Information of SUNSCREEN
| NDC Code | 66538-101-12 |
| Proprietary Name | SUNSCREEN |
| Package Description | 50 g in 1 JAR (66538-101-12) |
| Product NDC | 66538-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111128 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | COSMOCEUTICAL RESEARCH CENTER INC |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 7.5; 6 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
