Label: ESTRO-LIFT DAY THERAPY MOISTURIZER AND SPF 30 SUNSCREEN- octinoxate, octisalate, oxybenzone, and titanium dioxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 64483-378-01 - Packager: Clientele, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 10, 2019
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
- Directions
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Inactive Ingredients
Aqua/Water, Glycol Stearate SE, Propylene Glycol, Cetyl Alcohol, Aloe Barbadensis Leaf Juice, Cetearyl Alcohol, Dicetyl Phosphate, Ceteth-10 Phosphate, DEA-Cetyl Phosphate, Acetyl Glucosamine, Saccharide Isomerate, Sodium Hyaluronate, Butylene Glycol, Centella Asiatica Extract, Echinacea Purpurea Extract, Squalane, Panthenol, Tocopheryl Acetate, Nelumbo Nucifera (Sacred Lotus) Seed Extract1, Camellia Sinensis Leaf Extract, Pinus Strobus Bark Extract, Vitis Vinifera (Grape) Seed Extract, Glycerin, Catalase, Superoxide Dismutase, Cyclomethicone, Sodium Carboxymethyl Beta-Glucan, Magnesium Ascorbyl Phosphate, Hydrolyzed Soy Flour, Ubiquinone, Soy Isoflavones, Retinyl Palmitate, Cholecalciferol, Beta-Carotene, Diazolidinyl Urea, Methylparaben, Propylparaben, Hydroxyethylcellulose, Tetrasodium EDTA.
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- U.S. Patent #5,925,348 & #6,468,564.
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PRINCIPAL DISPLAY PANEL - 34 g Jar Label
Newly Improved Formula
Estro-Lift®
Day Therapy
Moisturizer & SPF 30 SunscreenHelps protect skin from photo-aging & sun damage with SPF 30.
Firming plant extracts are combined with powerful antioxidants,
vitamins, enzymes, and Clientele's age-defying Sacred Lotus Seed
Extract to moisturize, firm, and beautify your skin.CLIENTELE®
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INGREDIENTS AND APPEARANCE
ESTRO-LIFT DAY THERAPY MOISTURIZER AND SPF 30 SUNSCREEN
octinoxate, octisalate, oxybenzone, and titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64483-378 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 7000 mg in 1000 g Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 2000 mg in 1000 g Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 3000 mg in 1000 g Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP) Titanium Dioxide 1600 mg in 1000 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycol Stearate SE (UNII: 6YLY96TQL6) PPG-30 CETYL ETHER (UNII: 00C2W8NVII) Cetyl Alcohol (UNII: 936JST6JCN) ALOE VERA LEAF (UNII: ZY81Z83H0X) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) Ceteth-10 Phosphate (UNII: 4E05O5N49G) DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S) DISODIUM ACETYL GLUCOSAMINE PHOSPHATE (UNII: SC89MF712W) Saccharide Isomerate (UNII: W8K377W98I) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Butylene Glycol (UNII: 3XUS85K0RA) Centella Asiatica (UNII: 7M867G6T1U) Echinacea Purpurea (UNII: QI7G114Y98) Squalane (UNII: GW89575KF9) Panthenol (UNII: WV9CM0O67Z) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) NELUMBO NUCIFERA SEED (UNII: YCT65RT6AE) GREEN TEA LEAF (UNII: W2ZU1RY8B0) PINUS STROBUS BARK (UNII: 8PJ4761097) VITIS VINIFERA SEED (UNII: C34U15ICXA) Glycerin (UNII: PDC6A3C0OX) CATALASE (BOS TAURUS) (UNII: A7I0CI22DA) SUPEROXIDE DISMUTASE (SACCHAROMYCES CEREVISIAE) (UNII: W2T4YRA9AD) Cyclomethicone (UNII: NMQ347994Z) SODIUM CARBOXYMETHYL .BETA.-GLUCAN (DS 0.65-0.85) (UNII: 2YGO1190AP) Magnesium Ascorbyl Phosphate (UNII: 0R822556M5) SOYBEAN (UNII: L7HT8F1ZOD) UBIDECARENONE (UNII: EJ27X76M46) Soy Isoflavones (UNII: 71B37NR06D) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) Cholecalciferol (UNII: 1C6V77QF41) BETA CAROTENE (UNII: 01YAE03M7J) Methylparaben (UNII: A2I8C7HI9T) Propylparaben (UNII: Z8IX2SC1OH) HYDROXYETHYL ETHYLCELLULOSE (UNII: ZDN57Z154K) EDETATE SODIUM (UNII: MP1J8420LU) Diazolidinyl Urea (UNII: H5RIZ3MPW4) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64483-378-01 1 in 1 BOX 10/01/2002 1 34 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part352 04/01/1993 Labeler - Clientele, Inc. (085021806)