| Product NDC: | 76344-7001 |
| Proprietary Name: | MediSpa Sunblock SPF47 |
| Non Proprietary Name: | Octinoxate, Zinc Oxide, Avobenzone |
| Active Ingredient(s): | .5; 7; 5 g/100mL; g/100mL; g/100mL & nbsp; Octinoxate, Zinc Oxide, Avobenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76344-7001 |
| Labeler Name: | Humex,Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130422 |
| Package NDC: | 76344-7001-2 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (76344-7001-2) > 70 mL in 1 BOTTLE, PLASTIC (76344-7001-1) |
| NDC Code | 76344-7001-2 |
| Proprietary Name | MediSpa Sunblock SPF47 |
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (76344-7001-2) > 70 mL in 1 BOTTLE, PLASTIC (76344-7001-1) |
| Product NDC | 76344-7001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Zinc Oxide, Avobenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130422 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Humex,Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; ZINC OXIDE |
| Strength Number | .5; 7; 5 |
| Strength Unit | g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |