Home > Drugs A-Z > EltaMD UV Facial

EltaMD UV Facial (Swiss-American Products)

Available Formats

Dosage Form Package Information Links
LOTION 114 g in 1 JAR (60232-2283-4) Label Information
LOTION 86 g in 1 TUBE (60232-2283-3) Label Information

Complete EltaMD UV Facial Information

  • ACTIVE INGREDIENT

    Active Ingredients Purpose

    Octinoxate 7.5%.............UVB Sunscreen

    Zinc Oxide 7.0%.....UVA/UVB Sunscreen


  • INDICATIONS & USAGE

    EltaMD UV Facial SPF 30+ is a light, creamy, cosmetically elegant moisturizing sunscreen. It is specifically formulated to provide moisturizing UVA/UVB protection for the face, either alone or under makeup. For all skin types, especially moderate to dry skin types. EltaMD UV Facial is ideal after microdermabrasion, IPL treatments, chemical or glycolic peels and laser procedures.

    EltaMD UV Facial SPF 30+ is formulated with a transparent micronized zinc oxide that provides broad spectrum protection from both the UVA (aging) and UVB (burning) rays. It is non-comedogenic, sensitivity-free and fragrance-free.


  • WARNINGS

    WarningsFor external use only

    - Avoid direct contact with the eyes.
    - Discontinue use if signs of irritation appear.
    - Children under 6 months of age, consult your doctor.


  • WHEN USING

    Directions

    - Apply daily to face, neck and backs of hands, 30 minutes before exposure to the sun.


  • INACTIVE INGREDIENT

    Inactive Ingredients

    Purified Water, Petrolatum, Isopropyl Palmitate, Octyl Stearate, Cetearyl Glucoside, Glyceryl Stearate, Dimethicone, PEG-100 Stearate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyisobutene, PEG-7 Trimethylolpropane Coconut Ether, Sodium Hyaluronate, Tocopheryl Acetate, Polyether-1, Citric Acid, Oleth-3 Phosphate, Phenoxyethanol, Butylene Glycol, Iodopropynyl Butylcarbamate, Triethoxycaprylylsilane


  • PRINCIPAL DISPLAY PANEL

    Enter section text here Image of Tube Label


  • INGREDIENTS AND APPEARANCE
    ELTAMD UV FACIAL  SPF 30
    zinc oxide, octinoxate lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:60232-2283
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 75 g  in 1000 g
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 70 g  in 1000 g
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    Petrolatum (UNII: 4T6H12BN9U)  
    Isopropyl Palmitate (UNII: 8CRQ2TH63M)  
    Octyl Stearate (UNII: 772Y4UFC8B)  
    Cetearyl Glucoside (UNII: 09FUA47KNA)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    Dimethicone (UNII: 92RU3N3Y1O)  
    PEG-100 Stearate (UNII: YD01N1999R)  
    2-HYDROXYETHYL ACRYLATE (UNII: 25GT92NY0C)  
    SODIUM ACRYLOYLDIMETHYLTAURATE (UNII: 2T9Q6EKI0G)  
    POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)  
    COCONUT ALCOHOL (UNII: 13F4MW8Y9K)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Citric Acid monohydrate (UNII: 2968PHW8QP)  
    Oleth-3 Phosphate (UNII: 8Q0Z18J1VL)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)  
    Triethoxycaprylylsilane (UNII: LDC331P08E)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:60232-2283-4 114 g in 1 JAR
    2 NDC:60232-2283-3 86 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 04/30/2002
    Labeler - Swiss-American Products (611921669)
    Registrant - Swiss-American Products (611921669)
    Establishment
    Name Address ID/FEI Business Operations
    Swiss-American Products 611921669 manufacture