Product NDC: | 76214-037 |
Proprietary Name: | RED ORANGE SUN PACT |
Non Proprietary Name: | OCTINOXATE |
Active Ingredient(s): | .66; .29; .27 g/9.5g; g/9.5g; g/9.5g & nbsp; OCTINOXATE |
Administration Route(s): | CUTANEOUS |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76214-037 |
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: | 76214-037-01 |
Package Description: | 9.5 g in 1 CARTON (76214-037-01) |
NDC Code | 76214-037-01 |
Proprietary Name | RED ORANGE SUN PACT |
Package Description | 9.5 g in 1 CARTON (76214-037-01) |
Product NDC | 76214-037 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE |
Dosage Form Name | POWDER |
Route Name | CUTANEOUS |
Start Marketing Date | 20110301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SKINFOOD CO., LTD. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | .66; .29; .27 |
Strength Unit | g/9.5g; g/9.5g; g/9.5g |
Pharmaceutical Classes |