Label: ABIB HEARTLEAF MILD SUNSCREEN RELIEF TUBE- zinc oxide cream

  • NDC Code(s): 73676-217-01, 73676-217-02
  • Packager: FOURCOMPANY CO., LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 7, 2025

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

  • ACTIVE INGREDIENT

    Active ingredient(s)

    Zinc Oxide 19.32%

  • PURPOSE

    Purpose

    Sunscreen

  • INDICATIONS & USAGE

    Use(s)

    ■ Helps 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

    Warnings

    ■ For external use only

    ■ Do not use on damaged or broken skin

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

    ■ Stop use and ask a doctor if rash occurs

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

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Directions

    ■ Apply liberally and evenly 15 minutes before sun exposure

    ■ Reapply at least every 2 hours

    ■ Use a water-resistant sunscreen if swimming or sweating

    ■ Children under 6 months of age: Ask a doctor

    ■ 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 value of 15 or higher and other sun protection measures including:

    ■ Limit time in the sun, especially from 10 a.m. ‒ 2 p.m.

    ■ Wear long-sleeved shirts, pants, hats, and sunglasses

  • OTHER SAFETY INFORMATION

    Other Information

    ■ Protect the product in this container from excessive heat and direct sun

  • QUESTIONS

    Questions

    ■ contact@fourco.co.kr

  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Butyloctyl Salicylate, Propylheptyl Caprylate, Propanediol, C15-19 Alkane, Disiloxane, Isododecane, Cetyl Diglyceryl Tris(Trimethylsiloxy)silylethyl Dimethicone, Caprylyl Methicone, Isopropyl Myristate, Sodium Chloride, Triethylhexanoin, Glycerin, Disteardimonium Hectorite, Methyl Methacrylate Crosspolymer, Polymethylsilsesquioxane, Triethoxycaprylylsilane, 1,2-Hexanediol, Dipentaerythrityl Tri-Polyhydroxystearate, Houttuynia Cordata Extract, Lauryl Dimethicone/Polyglycerin-3 Crosspolymer, Polyglyceryl-2 Dipolyhydroxystearate, Panthenol, Caprylyl Glycol, Glyceryl Caprylate, Melia Azadirachta Leaf Extract, Melia Azadirachta Flower Extract, Coccinia Indica Fruit Extract, Butylene Glycol, Amber Powder, Solanum Melongena (Eggplant) Fruit Extract, Curcuma Longa (Turmeric) Root Extract, Dipropylene Glycol, Ocimum Sanctum Leaf Extract, Corallina Officinalis Extract, Moringa Oleifera Seed Oil, Tocopherol, Sodium Citrate, Lecithin, Sodium Hyaluronate, Allantoin, Dipotassium Glycyrrhizate, Sodium PCA, Arginine, Ceramide NP, Erythritol, Asiaticoside, Madecassic Acid, Asiatic Acid, Centella Asiatica Extract, Pentylene Glycol, Octanediol

  • PRINCIPAL DISPLAY PANEL

    Carton Image

  • INGREDIENTS AND APPEARANCE
    ABIB HEARTLEAF MILD SUNSCREEN RELIEF TUBE 
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73676-217
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION19.32 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    WATER (UNII: 059QF0KO0R)  
    ISODODECANE (UNII: A8289P68Y2)  
    HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    CETYL DIGLYCERYL TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE (950 MM2/S) (UNII: C982F2EKT3)  
    DIPENTAERYTHRITYL TRI-POLYHYDROXYSTEARATE (UNII: D21K655H52)  
    C15-19 ALKANE (UNII: CI87N1IM01)  
    CAPRYLYL METHICONE (UNII: Q95M2P1KJL)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    DISILOXANE (UNII: D7M4659BPU)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
    PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73676-217-021 in 1 CARTON05/01/2025
    1NDC:73676-217-0150 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/01/2025
    Labeler - FOURCOMPANY CO., LTD. (694864584)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosmax, Inc.689049693manufacture(73676-217)