| Product NDC: | 75916-0659 |
| Proprietary Name: | Snow Skin Sunscreen Lip Balm |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTOCRYLENE |
| Active Ingredient(s): | 2.5; 7.5; 5 g/100g; g/100g; g/100g & nbsp; AVOBENZONE, OCTINOXATE, OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75916-0659 |
| 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 NDC: | 75916-0659-8 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 BOX (75916-0659-8) > 8.5 g in 1 TUBE, WITH APPLICATOR |
| NDC Code | 75916-0659-8 |
| Proprietary Name | Snow Skin Sunscreen Lip Balm |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 BOX (75916-0659-8) > 8.5 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 75916-0659 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, OCTOCRYLENE |
| 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 | AVOBENZONE; OCTINOXATE; OCTOCRYLENE |
| Strength Number | 2.5; 7.5; 5 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |