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 |