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 |