Product NDC: | 59886-308 |
Proprietary Name: | UltrasolSunscreen |
Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, Oxybenzone |
Active Ingredient(s): | 2; 7.5; 3; 3 g/100g; g/100g; g/100g; g/100g & nbsp; Avobenzone, Octinoxate, Octisalate, Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59886-308 |
Labeler Name: | Fischer Pharmaceuticals Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100401 |
Package NDC: | 59886-308-55 |
Package Description: | 250 g in 1 BOTTLE, PLASTIC (59886-308-55) |
NDC Code | 59886-308-55 |
Proprietary Name | UltrasolSunscreen |
Package Description | 250 g in 1 BOTTLE, PLASTIC (59886-308-55) |
Product NDC | 59886-308 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100401 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Fischer Pharmaceuticals Ltd |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 2; 7.5; 3; 3 |
Strength Unit | g/100g; g/100g; g/100g; g/100g |
Pharmaceutical Classes |