Product NDC: | 51141-0301 |
Proprietary Name: | ATOPALM BB MEDIUM SPF 20 BROAD SPECTRUM SUNSCREEN |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
Active Ingredient(s): | 7.5; 8 g/100g; g/100g & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51141-0301 |
Labeler Name: | Neopharm Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120802 |
Package NDC: | 51141-0301-2 |
Package Description: | 1 TUBE in 1 CARTON (51141-0301-2) > 68 g in 1 TUBE |
NDC Code | 51141-0301-2 |
Proprietary Name | ATOPALM BB MEDIUM SPF 20 BROAD SPECTRUM SUNSCREEN |
Package Description | 1 TUBE in 1 CARTON (51141-0301-2) > 68 g in 1 TUBE |
Product NDC | 51141-0301 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120802 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Neopharm Co., Ltd. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 7.5; 8 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |