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SurfersSkin Sunscreen Zinc
SurfersSkin Sunscreen Zinc - 75916-0636-1 - (OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE)
Drug Information of SurfersSkin Sunscreen Zinc
| Product NDC: | 75916-0636 |
| Proprietary Name: | SurfersSkin Sunscreen Zinc |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE |
| Active Ingredient(s): | 7.5; 2.35; 4.2 g/100g; g/100g; g/100g & nbsp; OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SurfersSkin Sunscreen Zinc
| Product NDC: | 75916-0636 |
| Labeler Name: | Skin Alive, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110127 |
Package Information of SurfersSkin Sunscreen Zinc
| Package NDC: | 75916-0636-1 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 BOX (75916-0636-1) > 8.5 g in 1 TUBE, WITH APPLICATOR |
NDC Information of SurfersSkin Sunscreen Zinc
| NDC Code | 75916-0636-1 |
| Proprietary Name | SurfersSkin Sunscreen Zinc |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 BOX (75916-0636-1) > 8.5 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 75916-0636 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110127 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Skin Alive, Ltd. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7.5; 2.35; 4.2 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
