Label: 111 SKIN SUNSCREEN SPF 50- zinc oxide solution

  • NDC Code(s): 54111-190-01, 54111-190-02
  • Packager: Bentley Laboratories, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 23, 2026

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Drug Facts

    Active Ingredients

    Zinc Oxide 19.5%

  • PURPOSE

    Purpose

    Sunscreen

  • INDICATIONS & USAGE

    Uses

    • Helps prevent sunburn
    • If used as directed with other sun protection

    measures (see Directions), decreases the risk

    of skin cancer and early aging caused

    by the sun.

  • WARNINGS

    Warnings

    Do not use on damaged or broken skin.

    For external use only.

    When using this product keep out of eyes.

    If product gets into the eyes, rinse with water to remove

    Stop use and consult a doctor if rash occurs.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Directions
    • Apply generously and evenly to face and
    neck 15-20 minutes before sun exposure.
    • Reapply at least every 2 hours
    • Use a water-resistant sunscreen when
    swimming or sweating. • Sun Protection
    Measures. Spending time in the sun increases
    your risk of skin cancer and early aging.
    To reduce this risk, regularly use a sunscreen
    with a Broad Spectrum SPF value of 15 or higher
    and other sun protection measures including:
       - Limiting time in the sun, especially from 10 a.m. - 2 p.m.
    - Wear long-sleeved shirts, pants, hats, and sunglasses.
    • Children under 6 months: Ask a doctor.

  • OTHER SAFETY INFORMATION

    Other Information

    • Protect this product from excessive heat and direct sun.

  • INACTIVE INGREDIENT

    Inactive ingredients/Ingredients inactifs
    Isododecane, Water (Aqua/Eau), Coco-Caprylate/
    Caprate, Caprylyl Methicone, Propanediol,
    Glycerin, Polyglyceryl-4 Diisostearate/
    Polyhydroxystearate/Sebacate, Cetyl PEG/
    PPG-10/1 Dimethicone, Methyl Dihydroabietate,
    Tapioca Starch, Argania Spinosa Kernel Oil,
    Sodium Chloride, Tocopheryl Acetate,
    Dimethicone, Ethyl Ferulate, Disteardimonium
    Hectorite, Glycine Soja (Soybean) Oil,
    Hydroxyacetophenone, Isopentyldiol, Zinc
    Stearate, Propylene Carbonate, Physales
    Pubescens Fruit Juice, 1,2-Hexanediol, Caprylyl
    Glycol, Caprylic/Capric Triglyceride, Sodium
    Gluconate, Polyglyceryl-3 Diisostearate,
    Bisabolol, Escin, Fragrance (Parfum),
    Hydroxypropyl Cyclodextrin, Morus Alba Root
    Extract, Oryza Sativa (Rice) Extract, Oryza Sativa
    (Rice) Germ Extract, Tetrahexyldecyl Ascorbate,
    Polyglutamic Acid, Polyglyceryl-6 Laurate,
    Polycglyceryl-10 Oleate, Trifolium Pratense
    (Clover) Flower Extract Sorbitan Palmitate,
    Acetyl Cysteine, Soy Isoflavones,
    Glycosphingolipids, Tetramethyl
    Acetyloctahydronaphthalenes, Geranyl Acetate,
    Terpineol, Dimethyl Phenethyl Acetate.

  • Product Labeling:  111 SKIN SUNSCREEN SPF 50

    111SKIN

    HARLEY ST. LONDON

    SPF 50

    DR YANNIS ALEXANDRIDES

    SUNSCREEN

    SPF50

    ℮50mL./1.69 Fl.Oz.

    Made in the USA for:

    111 SKIN LTD

    111 Harley Street, London,

    WiG 6AW, UK

    www.111skin@111skin.com

    50 mL Carton

    50mL 111 Skin Box

    50 mL Bottle

    50mL 111 Skin Botl

    15 mL Carton

    15mL 111 Skin Box

    15 mL Bottle

    15mL 111 Skin Botl

    res

  • INGREDIENTS AND APPEARANCE
    111 SKIN SUNSCREEN SPF 50 
    zinc oxide solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54111-190
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION19.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISODODECANE (UNII: A8289P68Y2)  
    WATER (UNII: 059QF0KO0R)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    CAPRYLYL METHICONE (UNII: Q95M2P1KJL)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
    METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)  
    TAPIOCA STARCH (UNII: 24SC3U704I)  
    ARGANIA SPINOSA KERNEL OIL (UNII: 4V59G5UW9X)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ETHYL FERULATE (UNII: 5B8915UELW)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    GLYCINE SOJA (SOYBEAN) OIL UNSAPONIFIABLES (UNII: WZ7DY7GBV6)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    ISOPENTYLDIOL (UNII: 19NOL5474Q)  
    ZINC STEARATE (UNII: H92E6QA4FV)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    PHYSALIS PUBESCENS FRUIT JUICE (UNII: GM2TDN9DZI)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)  
    BISABOLOL (UNII: 24WE03BX2T)  
    ESCIN (UNII: RUU8G67GQM)  
    HYDROXYPROPYL BETADEX (UNII: 1I96OHX6EK)  
    MORUS ALBA ROOT (UNII: CST1G9BZGD)  
    RICE GERM (UNII: 7N2B70SFEZ)  
    RICE GERM OIL (UNII: D4H5GGS5JF)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    POLYGLUTAMIC ACID (1200 MW) (UNII: MGE3733FR2)  
    POLYGLYCERYL-6 LAURATE (UNII: Q48X4BL3TV)  
    POLYGLYCERYL-10 OLEATE (UNII: 55C81W76DH)  
    TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)  
    SORBITAN PALMITATE (UNII: 77K6Z421KU)  
    ACETYL CYSTEINE (UNII: WYQ7N0BPYC)  
    SOY ISOFLAVONES (UNII: 71B37NR06D)  
    HYDROXYETHYL PALMITYL OXYHYDROXYPROPYL PALMITAMIDE (UNII: ISA73Z2140)  
    TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES (UNII: 2JU6ZH6GRE)  
    GERANYL ACETATE (UNII: 3W81YG7P9R)  
    TERPINEOL (UNII: R53Q4ZWC99)  
    DIMETHYL BENZYL CARBINYL ACETATE (UNII: 6Y9488RL8H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54111-190-011 in 1 CARTON05/23/2025
    150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2NDC:54111-190-021 in 1 CARTON05/01/2026
    215 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/23/2025
    Labeler - Bentley Laboratories, LLC (068351753)