Label: ECLIPSE SPF 50 ALL SHADES- titanium dioxide, zinc oxide lotion

  • NDC Code(s): 69219-102-01, 69219-102-02, 69219-102-03, 69219-102-11, view more
    69219-102-13, 69219-102-21, 69219-102-51, 69219-102-53
  • Packager: SCIENCE OF SKINCARE LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 14, 2023

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  • Active Ingredients

    TITANIUM DIOXIDE – 5.20%

    Zinc Oxide – 1.10%

  • PURPOSE

    SUNSCREEN

  • USES

    • Helps hydrate and prevent sunburn.
    • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

  • WARNINGS

    • For external use only

  • DO NOT USE

    • Do not use on damaged or broken skin

  • WHEN USING

    • When using this product keep out of eyes. Rinse with water to remove

  • STOP USE

    • Stop use and ask a doctor if rash occurs

  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children. If product is swallowed,get medical help or contact a Poison Control Center right away.
  • DIRECTIONS

    • APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.
    • REAPPLY:
    • AFTER 40 MINUTES OF SWIMMING OR SWEATING
    • IMMEDIATELY AFTER TOWEL DRYING
    • AT LEAST EVERY 2 HOURS

    • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
    o limit time in the sun, especially from 10 a.m.-2 p.m.
    o wear long-sleeve shirts, pants, hats, and sunglasses
    • Children under 6 months: Ask a doctor

  • Other Information

    Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin cancer, and other harmful effects of the sun.

  • Questions or Comments?

    Call Customer Care at (888) 804-4447

  • Inactive Ingredients

    1,2-Hexanediol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Alumina, Butylene Glycol, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cetearyl Alcohol, Cetearyl Glucoside, Disodium EDTA, Dimethicone, Glyceryl Stearate, Methicone, Octyldodecyl Neopentanoate, PEG-100 Stearate, Polyhydroxystearic Acid, Sorbitan Laurate, Styrene/Acrylates Copolymer, Tocopherol, Tocopheryl Acetate, Triethoxycaprylylsilane, VP/Eicosene Copolymer, Water/Aqua/Eau, Xanthan Gum +/- Iron Oxides.

  • Package Label - Principal Display Panel

    300g Box NDC 69219-102-5310g Bag NDC 69219-102-21100g Label NDC 69219-102-01300g Label NDC 69219-102-03100g Box NDC 69219-102-1110g Label NDC 69219-102-02

  • INGREDIENTS AND APPEARANCE
    ECLIPSE SPF 50  ALL SHADES
    titanium dioxide, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69219-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE5.2 g  in 100 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION1.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    ALUMINUM (UNII: CPD4NFA903)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)  
    STYRENE (UNII: 44LJ2U959V)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69219-102-511 in 1 BOX10/01/2014
    1NDC:69219-102-1390 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2NDC:69219-102-111 in 1 BOX10/01/2014
    2NDC:69219-102-01100 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    3NDC:69219-102-211 in 1 BAG10/01/2014
    3NDC:69219-102-0210 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    4NDC:69219-102-03300 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2014
    5NDC:69219-102-01100 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2014
    6NDC:69219-102-0210 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2014
    7NDC:69219-102-531 in 1 BOX08/01/2023
    7300 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/01/2014
    Labeler - SCIENCE OF SKINCARE LLC (006251958)
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