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 |