| 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 |