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SnowSkin Face Sunscreen
SnowSkin Face Sunscreen - 75916-0641-4 - (OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE)
Drug Information of SnowSkin Face Sunscreen
| Product NDC: | 75916-0641 |
| Proprietary Name: | SnowSkin Face Sunscreen |
| Non Proprietary Name: | OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE |
| Active Ingredient(s): | 6; 3.3; 14.25 g/100g; g/100g; g/100g & nbsp; OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SnowSkin Face Sunscreen
| Product NDC: | 75916-0641 |
| Labeler Name: | Skin Alive, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110117 |
Package Information of SnowSkin Face Sunscreen
| Package NDC: | 75916-0641-4 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 BOX (75916-0641-4) > 40 g in 1 TUBE, WITH APPLICATOR |
NDC Information of SnowSkin Face Sunscreen
| NDC Code | 75916-0641-4 |
| Proprietary Name | SnowSkin Face Sunscreen |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 BOX (75916-0641-4) > 40 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 75916-0641 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110117 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Skin Alive, Ltd. |
| Substance Name | OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 6; 3.3; 14.25 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
