| Product NDC: | 51141-0300 |
| Proprietary Name: | ATOPALM BB LIGHT 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: | 51141-0300 |
| 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: | 51141-0300-2 |
| Package Description: | 1 TUBE in 1 CARTON (51141-0300-2) > 68 g in 1 TUBE |
| NDC Code | 51141-0300-2 |
| Proprietary Name | ATOPALM BB LIGHT SPF 20 BROAD SPECTRUM SUNSCREEN |
| Package Description | 1 TUBE in 1 CARTON (51141-0300-2) > 68 g in 1 TUBE |
| Product NDC | 51141-0300 |
| 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 |