Label: CRATIV SUNSCREEN- ethylhexyl methoxycinnamate,titanium dioxide, homosalate, ethylhexyl, salicylate, octocrylene, bis-ethylhexyloxyphenolmethoxyphenyltriazine,4-methylbenzylidene camphor, dimethicone,butyl methoxydibenzoylmethane lotion

  • NDC Code(s): 84301-001-01
  • Packager: Foshan Xinhai Jiayu Import and Export Trade Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 11, 2024

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

  • ACTIVE INGREDIENT

    Ethylhexyl methoxycinnamate 10%
    Titanium dioxide 4.5%
    Homosalate 6%
    Ethylhexyl salicylate 4.5%
    Octocrylene 2.9%
    Bis-ethylhexyloxyphenolmethoxyphenyltriazine 2%
    4-methylbenzylidene camphor 0.5%
    DIMETHICONE 1%
    Butyl methoxydibenzoylmethane 1%

  • PURPOSE

    Protecting the skin from the damagecaused by ultraviolet (UV) radiation. UVrays can lead to skin sunburn, sunburnerythema, skin cancer, and other issuesBy forming a protective layer on the skinsurface, sunscreen blocks, absorbs,orreflects UV radiation, thus reducing itsharmful effects on the skin.

  • INDICATIONS & USAGE

    Protecting the skin from the damagecaused by ultraviolet (UV) radiation. UVrays can lead to skin sunburn, sunburnerythema, skin cancer, and other issuesBy forming a protective layer on the skinsurface, sunscreen blocks, absorbs,orreflects UV radiation, thus reducing itsharmful effects on the skin.

  • WARNINGS

    For external use only

  • DO NOT USE

    5. Do not use when the skinhas abnormal conditions. This producthas passed the quality test, but it doesnot mean that very few people will nothave adverse reactions such as allergies.lf anything abnormal occurs during usediscontinue use immediately and cons-ult your doctor if necessary

  • WHEN USING

    1. Do not place in sunlightand high temperatures,do not swallow.2. Keep out of reach of the baby. 3. O-pen the bag and use it. 4. In case of c-ontact with eyes, rinse immediatelywith water.

  • STOP USE

    5. Do not use when the skinhas abnormal conditions. This producthas passed the quality test, but it doesnot mean that very few people will nothave adverse reactions such as allergies.lf anything abnormal occurs during usediscontinue use immediately and cons-ult your doctor if necessary

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of the baby.

  • DOSAGE & ADMINISTRATION

    Step 1: Cleanse. Start with clean and dryskin. Wash your face and any exposedareas gently to remove dirt and sweat.
    Step 2: Apply Before Sun Exposure. Applysunscreen generously at least 15 minutesbefore going out in the sun. This allowsyour skin to absorb the product properly.
    Step 3: Amount Matters. Use enough s-unscreen to cover all exposed skin. As ageneral guide, apply about a teaspoon(5ml) to your face and a shot glass wort-h for your body.
    Step 4: Even Application. Spread the su-nscreen evenly over your skin. Don't for-get easily overlooked areas like ears, ne-ck, and the back of your hands.
    Step 5: Reapply. Reapply sunscreen eve-ry two hours, or more often if you're sw-eating heavily or swimming. Even water-resistant' sunscreen can wear off.

  • STORAGE AND HANDLING

    1. Do not place in sunlightand high temperatures,do not swallow.2. Keep out of reach of the baby.

  • INACTIVE INGREDIENT

    water
    propylene glycol
    C12-15 Alcohol Benzoate
    cyclopentasiloxane
    Caprylic/capric triglyceride
    PEG-30 Dipolyhydroxystearate
    Sodium chloride
    MONTMORILLONITE
    Sorbitan oleate
    Phenoxyethanol
    .ALPHA.-TOCOPHEROL
    SILICON DIOXIDE
    Methylparaben
    CETYL PHOSPHATE
    Propylparaben
    Ethylhexylglycerin
    Sodium hyaluronate

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CRATIV SUNSCREEN 
    ethylhexyl methoxycinnamate,titanium dioxide, homosalate, ethylhexyl, salicylate, octocrylene, bis-ethylhexyloxyphenolmethoxyphenyltriazine,4-methylbenzylidene camphor, dimethicone,butyl methoxydibenzoylmethane lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84301-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE2.9 g  in 100 mL
    BEMOTRIZINOL (UNII: PWZ1720CBH) (BEMOTRIZINOL - UNII:PWZ1720CBH) BEMOTRIZINOL2 g  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE6 g  in 100 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE4.5 g  in 100 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE10 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 mL
    ENZACAMENE (UNII: 8I3XWY40L9) (ENZACAMENE - UNII:8I3XWY40L9) ENZACAMENE0.5 g  in 100 mL
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MONTMORILLONITE (UNII: A585MN1H2L)  
    CETYL PHOSPHATE (UNII: VT07D6X67O)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    WATER (UNII: 059QF0KO0R)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84301-001-0150 mL in 1 TUBE; Type 0: Not a Combination Product05/11/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/11/2024
    Labeler - Foshan Xinhai Jiayu Import and Export Trade Co., Ltd (412478748)
    Establishment
    NameAddressID/FEIBusiness Operations
    Foshan Xinhai Jiayu Import and Export Trade Co., Ltd412478748manufacture(84301-001)