Product NDC: | 76214-027 |
Proprietary Name: | ALOE SUN BB |
Non Proprietary Name: | TITANIUM DIOXIDE |
Active Ingredient(s): | 1.5; 3.86 g/50g; g/50g & nbsp; TITANIUM DIOXIDE |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76214-027 |
Labeler Name: | SKINFOOD CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110301 |
Package NDC: | 76214-027-01 |
Package Description: | 50 g in 1 CARTON (76214-027-01) |
NDC Code | 76214-027-01 |
Proprietary Name | ALOE SUN BB |
Package Description | 50 g in 1 CARTON (76214-027-01) |
Product NDC | 76214-027 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | CUTANEOUS |
Start Marketing Date | 20110301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SKINFOOD CO., LTD. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 1.5; 3.86 |
Strength Unit | g/50g; g/50g |
Pharmaceutical Classes |