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SnowSkin Sunscreen
SnowSkin Sunscreen - 75916-4018-1 - (OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE)
Drug Information of SnowSkin Sunscreen
| Product NDC: | 75916-4018 |
| Proprietary Name: | SnowSkin Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
| Active Ingredient(s): | 7.5; 3.45; 1; 1.95 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SnowSkin Sunscreen
| Product NDC: | 75916-4018 |
| Labeler Name: | Skin Alive, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110105 |
Package Information of SnowSkin Sunscreen
| Package NDC: | 75916-4018-1 |
| Package Description: | 40 mL in 1 TUBE (75916-4018-1) |
NDC Information of SnowSkin Sunscreen
| NDC Code | 75916-4018-1 |
| Proprietary Name | SnowSkin Sunscreen |
| Package Description | 40 mL in 1 TUBE (75916-4018-1) |
| Product NDC | 75916-4018 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110105 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Skin Alive, Ltd. |
| Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7.5; 3.45; 1; 1.95 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
