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UVA/UVB SPF 15
UVA/UVB SPF 15 - 14222-2022-2 - (Octinoxate, Zinc Oxide)
Drug Information of UVA/UVB SPF 15
| 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) |
Labeler Information of UVA/UVB SPF 15
| 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 Information of UVA/UVB SPF 15
| Package NDC: | 14222-2022-2 |
| Package Description: | 1 BOTTLE in 1 BOX (14222-2022-2) > 50 mL in 1 BOTTLE (14222-2022-1) |
NDC Information of UVA/UVB SPF 15
| 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 |
