| Product NDC: | 59779-301 |
| Proprietary Name: | age renewal firming and hydrating moisturizer |
| Non Proprietary Name: | Octinoxate, Octisalate, Oxybenzone, Zinc Oxide |
| Active Ingredient(s): | .075; .05; .04; .02 g/g; g/g; g/g; g/g & nbsp; Octinoxate, Octisalate, Oxybenzone, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59779-301 |
| Labeler Name: | Woonsocket Prescription Center, Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091222 |
| Package NDC: | 59779-301-01 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (59779-301-01) > 51 g in 1 BOTTLE, GLASS |
| NDC Code | 59779-301-01 |
| Proprietary Name | age renewal firming and hydrating moisturizer |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (59779-301-01) > 51 g in 1 BOTTLE, GLASS |
| Product NDC | 59779-301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Oxybenzone, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20091222 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Woonsocket Prescription Center, Incorporated |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; ZINC OXIDE |
| Strength Number | .075; .05; .04; .02 |
| Strength Unit | g/g; g/g; g/g; g/g |
| Pharmaceutical Classes |