Label: LIKEWISE FACIAL MOISTURIZER - SUN PROTECTANT SPF 50 OILY SKIN- titanium dioxide, zinc oxide cream
- NDC Code(s): 76229-234-02
- Packager: Likewise Incorporated
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- Uses
- WARNINGS
- WHEN USING
- STOP USE
- Keep out of reach of children.
- OTHER SAFETY INFORMATION
- DOSAGE & ADMINISTRATION
- PRECAUTIONS
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INACTIVE INGREDIENT
Inactive ingredients Water (Aqua), Cyclopentasiloxane, Cyclohexasiloxane, PEG-10 Dimethicone, Butylene Glycol, Alumina, Polyglyceryl-6 Polyricinoleate, Cetyl Dimethicone, Cetyl Hydroxyethylcellulose, Sodium Chloride, Azelaic Acid, Genistein, Niacinamide, Tocopherol, Disteardimonium Hectorite, Polyglyceryl-2 Isostearate, Dimethicone, Methicone, Triethoxycaprylylsilane, 1,2-Hexanediol, Caprylyl Glycol, Glycerin, Moringa Pterygosperma Seed Extract, Secale Cereale (Rye) Seed Extract, Dextrin, Ectoin, Atelocollagen, Chlorphenesin, Phyllanthus Emblica Fruit Extract, Lecithin, Xanthan Gum, Sodium Chondroitin Sulfate, Algin, Sodium Citrate, Serine, Caprylic/Capric Triglyceride, Ascorbyl Tetraisopalmitate, Carbomer, DNA, Vinyl Dimethicone Crosspolymer, Ethylbisiminomethylguaiacol Manganese Chloride, Cyclomethicone.
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DESCRIPTION
OILY SKIN Daily moisturizer + Sunscreen Dermatologist developed Mattifying balancer controls oil and blemishes with Azelaic Acid and Niacinamide Anti-aging antioxidants reverse daily damage and rejuvenate skin Contains Vitamins B, C and E and Natural Soy to improve skin tone and texture Works wonders as a nightime moisturizer, too Non-greasy light coverage (apply 1 pea-size dop) Delightfully fragrance free LikewiseSkinCare.com LIKEWISE INCORPORATED 200 COOL SPRINGS BOULEVARD FRANKLIN, TENNESSEE 37067 IN CASE OF ADVERSE REACTION: 877.778.9546
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INGREDIENTS AND APPEARANCE
LIKEWISE FACIAL MOISTURIZER - SUN PROTECTANT SPF 50 OILY SKIN
titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76229-234 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 65 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 66.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CYCLOMETHICONE 6 (UNII: XHK3U310BA) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ALUMINUM OXIDE (UNII: LMI26O6933) SODIUM CHLORIDE (UNII: 451W47IQ8X) AZELAIC ACID (UNII: F2VW3D43YT) GENISTEIN (UNII: DH2M523P0H) NIACINAMIDE (UNII: 25X51I8RD4) TOCOPHEROL (UNII: R0ZB2556P8) DIMETHICONE (UNII: 92RU3N3Y1O) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) MORINGA OLEIFERA SEED (UNII: TIX5482832) RYE (UNII: 0R4AQI398X) ICODEXTRIN (UNII: 2NX48Z0A9G) ECTOINE (UNII: 7GXZ3858RY) CHLORPHENESIN (UNII: I670DAL4SZ) PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A) SODIUM ALGINATE (UNII: C269C4G2ZQ) SODIUM CITRATE (UNII: 1Q73Q2JULR) SERINE (UNII: 452VLY9402) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) HERRING SPERM DNA (UNII: 51FI676N6F) CYCLOMETHICONE (UNII: NMQ347994Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76229-234-02 1 in 1 PACKAGE 12/19/2017 1 50 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/20/2011 Labeler - Likewise Incorporated (027215523) Establishment Name Address ID/FEI Business Operations Englewood Lab, Inc. 172198223 manufacture(76229-234)