Product NDC: | 14222-2022 |
Proprietary Name: | UVA/UVB SPF 15 |
Non Proprietary Name: | Octinoxate, Zinc Oxide |
Active Ingredient(s): | 7.5; 3.4 mL/100mL; mL/100mL & nbsp; Octinoxate, Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 14222-2022 |
Labeler Name: | Rodan & Fields LLC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110603 |
Package NDC: | 14222-2022-2 |
Package Description: | 1 BOTTLE in 1 BOX (14222-2022-2) > 50 mL in 1 BOTTLE (14222-2022-1) |
NDC Code | 14222-2022-2 |
Proprietary Name | UVA/UVB SPF 15 |
Package Description | 1 BOTTLE in 1 BOX (14222-2022-2) > 50 mL in 1 BOTTLE (14222-2022-1) |
Product NDC | 14222-2022 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Zinc Oxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110603 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Rodan & Fields LLC. |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 7.5; 3.4 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |