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 |