| Product NDC: | 15127-000 |
| Proprietary Name: | Select Brand Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | 7.5; 4.5 g/100g; g/100g & nbsp; OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 15127-000 |
| Labeler Name: | Select Brand Distributors |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121116 |
| Package NDC: | 15127-000-16 |
| Package Description: | 226 g in 1 BOTTLE, PLASTIC (15127-000-16) |
| NDC Code | 15127-000-16 |
| Proprietary Name | Select Brand Sunscreen |
| Package Description | 226 g in 1 BOTTLE, PLASTIC (15127-000-16) |
| Product NDC | 15127-000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121116 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Select Brand Distributors |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 7.5; 4.5 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |