Label: IHAVE SUNSCREEN- titanium dioxide, zinc oxide, ethylhexyl salicylate cream

  • NDC Code(s): 83566-501-01, 83566-501-02, 83566-501-03, 83566-501-04, view more
    83566-501-05, 83566-501-06
  • Packager: Guangdong Aimu Biological Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 9, 2024

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  • SPL UNCLASSIFIED SECTION

    ihave Sunscreen

  • ACTIVE INGREDIENT

    TITANIUM DIOXIDE 6%, ZINC OXIDE 6%, ETHYLHEXYL SALICYLATE 3%

  • PURPOSE

    Broad SpectrumUVA/UVB Protection

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • INDICATIONS & USAGE

    Directions: Apply liberally and evenly 15minutes before sun exposure.Reapply at least every 2 hours, or afterswimming, sweating, or towel drying

  • WARNINGS

    For external use only.

  • DOSAGE & ADMINISTRATION

    Directions: Apply liberally and evenly 15minutes before sun exposure.Reapply at least every 2 hours, or afterswimming, sweating,or towel drying

  • STORAGE AND HANDLING

    Store in a dark and cool place

  • INACTIVE INGREDIENT

    GLYCERIN
    TREHALOSE
    ALLANTOIN
    PAEONIA LACTIFLORA ROOT
    CETEARYL GLUCOSIDE
    CHLORPHENESIN
    MEADOWFOAM SEED OIL
    HYDROGENATED MACADAMIA SEED OIL
    WHEAT GERM OIL
    ASCORBIC ACID
    CETEARETH-22
    WATER
    NIACINAMIDE
    PROPYLENE GLYCOL
    HYALURONATE SODIUM
    DIMETHICONE
    CANNABIS SATIVA LEAF
    CETOSTEARYL ALCOHOL
    ALPHA-TOCOPHEROL ACETATE
    WHEAT GERM
    GLYCYRRHIZINATE DIPOTASSIUM
    ALKYL (C12-15) BENZOATE
    ETHYLHEXYLGLYCERIN
    1,3-BETA-GLUCAN SYNTHASE COMPONENT FKS1
    CENTELLA ASIATICA ROOT
    ALOE FEROX LEAF
    XANTHAN GUM
    LEVOMENOL

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    IHAVE SUNSCREEN 
    titanium dioxide, zinc oxide, ethylhexyl salicylate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83566-501
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE6 g  in 100 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE6 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    TREHALOSE (UNII: B8WCK70T7I)  
    ALLANTOIN (UNII: 344S277G0Z)  
    PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)  
    HYDROGENATED MACADAMIA SEED OIL (UNII: W4FFC8IM2K)  
    WHEAT GERM OIL (UNII: 14C97E680P)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    CETEARETH-22 (UNII: 28VZG1E234)  
    WATER (UNII: 059QF0KO0R)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CANNABIS SATIVA LEAF (UNII: A718Z7DA1K)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WHEAT GERM (UNII: YR3G369F5A)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    1,3-BETA-GLUCAN SYNTHASE COMPONENT FKS1 (UNII: 4FRY3LJG0V)  
    CENTELLA ASIATICA ROOT (UNII: 8MXU1P42J0)  
    ALOE FEROX LEAF (UNII: 0D145J8EME)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83566-501-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2024
    2NDC:83566-501-0240 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2024
    3NDC:83566-501-0350 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2024
    4NDC:83566-501-0460 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2024
    5NDC:83566-501-0580 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2024
    6NDC:83566-501-06100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/09/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02004/09/2024
    Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Aimu Biological Technology Co., Ltd712647107manufacture(83566-501)
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