Label: AROMA MATTE DAY SUNSCREEN SPF-30- octinoxate, octisalate, zinc oxide cream

  • NDC Code(s): 70764-208-52
  • Packager: CONTROL CORRECTIVE SKINCARE INC
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 22, 2023

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  • ACTIVE INGREDIENTS

    OCTINOXATE (6.9%)

    OCTISALATE (3.0%)

    ZINC OXIDE (4.0%)

  • PURPOSE

    SUNSCREEN

  • USE

    A MULTI-PURPOSE SUNSCREEN AND FACIAL MOISTURIZER. OFFERS BROAD SPECTRUM UVA & UVB PROTECTION WITHOUT LEAVING A GREASY FILM. HELPS PREVENT AGAINST TANNING AND BURNING. CONTAINS ALOE VERA AND ANTIOXIDANTS TO HELP SOOTHE AND BALANCE THE SKIN. MAY BE USED AS A FACIAL MOISTURIZER TO HELP FIGHT THE SIGNS OF AGING WHICH INCLUDES WRNKLING, DRYNESS, PIGMENTATION AND REDNESS.

  • WARNING

    FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT, AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER. DISCONTINUE USE AND ASK A DOCTOR IF IRRITATION OR RASH DEVELOPS.

  • DIRECTIONS

    APPLY TO CLEAN SKIN AT LEAST 15 MINUTES PRIOR TO SUN EXPOSURE. MAY BE USED AS OFTEN AS DESIRED. PENETRATES QUICKLY LEAVING A MATTE FINISH. SAFE FOR SENSITIVE SKIN.

  • OTHER SAFETY INFORMATION

    SUN ALERT: LIMITING SUN EXPOSURE, WEARING PROTECTIVE CLOTHING, AND USING SUNSCREEN MAY REDUCE THE RISK OF SKIN AGING, SKIN CANCER, AND OTHER HARMFUL EFFECTS OF THE SUN.

  • INACTIVE INGREDIENTS

    WATER, ALOE BARBADENSIS LEAF, GLYCERIN, PROPYLENE GLYCOL, ISOPROPYL PALMITATE, CAPRYLIC/CAPRIC TRIGLYCERIDES, CYCLOPENTASILOXANE, CETEARYL ALCOHOL, CETEARETH-20, VP/EICOSENE COPOLYMER, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, SQUALANE, POLYSORBATE 60, CYCLOTETRASILOXANE, PHENOXYETHANOL, FRAGRANCE, BUTYROSPERMUM PARKII SHEA BUTTER, PERSEA GRATISSIMA OIL, TOCOPHERYL ACETATE, DISODIUM EDTA, TRIETHOXYCAPRYLYLSILANE, ASPALATHUS LINEARIS LEAF EXTRACT, CAMELLIA OLEIFERA LEAF EXTRACT, DIPROPYLENE GLYCOL, BOSWELLIA SERRATA GUM, CITRIC ACID, METHYLISOTHIAZOLINONE, SODIUM ASCORBYL PHOSPHATE, CHOLECALCIFEROL

  • 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.

  • QUESTIONS OR COMMENTS

    WWW.CONTROLCORRECTIVE.COM

    TOLL FREE 1-866-290-4290  MADE IN USA

  • PRINCIPAL DISPLAY PANEL

    unit carton

  • INGREDIENTS AND APPEARANCE
    AROMA MATTE DAY   SUNSCREEN SPF-30
    octinoxate, octisalate, zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70764-208
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE6.9 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE3 g  in 100 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION4 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
    SQUALANE (UNII: GW89575KF9)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    AVOCADO OIL (UNII: 6VNO72PFC1)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)  
    CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    CYCLOMETHICONE 4 (UNII: CZ227117JE)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70764-208-521 in 1 BOX09/11/2018
    174 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02009/11/2018
    Labeler - CONTROL CORRECTIVE SKINCARE INC (023999357)