Label: GHH INVISIBLE PROTECTION DAILY SUNSCREEN- sunscreen cream

  • NDC Code(s): 75779-007-01
  • Packager: GUANG DONG 3 INS TECHNOLOGY Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 18, 2024

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

  • Active Ingredient

    Octocrylene 8%

  • Purpose

    Sunscreen

  • Use

    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

    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

  • Ask Doctor

    Children under 6 months of age: Ask a doctor

  • Keep Oot Of Reach Of Children

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

  • Directions

    For sunscreen use:
    apply liberally 15 minutes before sun exposure
    reapply at least every 2 hours
    reapply after 40 minites of swimming or sweating
    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
    Children under 6 months of age: Ask a doctor

  • Other information

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

  • Inactive ingredients

    Water,Ethylhexyl Methoxycinnamate,Homosalate,Butylene Glycol,C12-15 Alkyl Benzoate,Ethylhexyl Salicylate,Titanium Dioxide,Butyl Methoxydibenzoylmethane,Phenylbenzimidazole Sulfonic Acid,Cetearyl Alcohol,Glycerin,Diethylhexyl Carbonate,PEG-100 Stearate,Glyceryl Stearate,Cyclopentasiloxane,Dimethicone,Sodium Hydroxide,Phenoxyethanol,Polyacrylate-13,C20-22 Alkyl Phosphate,Hydrated Silica,C20-22 Alcohols,Hydroxyacetophenone,Polyisobutene,Dimethicone/Vinyl Dimethicone Crosspolymer,Aluminum Hydroxide,Hydrogen Dimethicone,1,2-Hexanediol,Tocopheryl Acetate,Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Fragrance,Bisabolol,Disodium Edta,Xanthan Gum,Polysorbate 20,Sorbitan Isostearate

  • Questions

    +8615899888175

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    GHH INVISIBLE PROTECTION DAILY SUNSCREEN 
    sunscreen cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75779-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE8 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    WATER (UNII: 059QF0KO0R)  
    HOMOSALATE (UNII: V06SV4M95S)  
    C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP)  
    DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
    DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    OCTINOXATE (UNII: 4Y5P7MUD51)  
    AVOBENZONE (UNII: G63QQF2NOX)  
    ENSULIZOLE (UNII: 9YQ9DI1W42)  
    HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    C20-22 ALCOHOLS (UNII: O4M0347C6A)  
    POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    FRAGRANCE 13576 (UNII: 5EM498GW35)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    OCTISALATE (UNII: 4X49Y0596W)  
    POLYACRYLATE-13 (UNII: FS2D4T67EA)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYOXYL 100 STEARATE (UNII: YD01N1999R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75779-007-0150 g in 1 BOTTLE; Type 0: Not a Combination Product06/18/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/18/2024
    Labeler - GUANG DONG 3 INS TECHNOLOGY Co., Ltd (552312961)
    Establishment
    NameAddressID/FEIBusiness Operations
    GUANG DONG 3 INS TECHNOLOGY Co., Ltd552312961manufacture(75779-007)