Product NDC: | 15127-006 |
Proprietary Name: | Select Brand Sunscreen |
Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
Active Ingredient(s): | 3; 15; 5; 10; 6 g/100g; g/100g; g/100g; g/100g; g/100g & nbsp; AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 15127-006 |
Labeler Name: | Select Brand Distributors |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121121 |
Package NDC: | 15127-006-16 |
Package Description: | 226 g in 1 BOTTLE, PLASTIC (15127-006-16) |
NDC Code | 15127-006-16 |
Proprietary Name | Select Brand Sunscreen |
Package Description | 226 g in 1 BOTTLE, PLASTIC (15127-006-16) |
Product NDC | 15127-006 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20121121 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Select Brand Distributors |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 3; 15; 5; 10; 6 |
Strength Unit | g/100g; g/100g; g/100g; g/100g; g/100g |
Pharmaceutical Classes |