Label: POST RAYS UV PROTECT SUN BLOCK- zinc oxide,octinoxate, octisalate,titamium dioxide cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 January 11, 2021

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  • Drug Facts Active Ingredient Purpose

    packaging with label in placeZinc Oxide (5.006%)-----------------------------Sunscreen
    Octinoxate (6.8%)--------------------------------Sunscreen
    Octisalate (4%)------------------------------------Sunscreen
    Titanium Dioxide (4.0014%)-------------------Sunscreen

  • Uses

    Helps prevent sunburn

  • Warnings

    Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

    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 (1-800-222-1222) right away.

  • Directions

    ▪ Apply liberally 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

  • Other Information

    ▪ protect the product in this container from excessive heat and direct sun

  • Inactive Ingredients

    water, cyclomethicone, methicone, aluminum hydroxide,dimethicone, dipropylene glycol, peg-10 dimethicone, glycerin, dicaprylyl carbonate, propanediol, saccharide hydrolysate(invert sugar), 1,2-hexandediol, salvia hispanica seed (chia seed) extract, curcuma longa (turmeric) root extract, caprylyl trisiloxane, disteardimonium hectorite, magnesium sulfate, dimethicone/vinyl dimethicone crosspolymer, caprylyl glycol, ethylhexylglycerin, glyceryl monocaprylate

  • PRINCIPAL DISPLAY PANEL

    a representative sample image of a carton/container label

  • INGREDIENTS AND APPEARANCE
    POST RAYS UV PROTECT SUN BLOCK 
    zinc oxide,octinoxate, octisalate,titamium dioxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76344-8002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE6.8 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE4.0014 g  in 100 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE5.006 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) 1 g  in 100 g
    MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) 0.8 g  in 100 g
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) 0.8 g  in 100 g
    TURMERIC (UNII: 856YO1Z64F) 0.01 g  in 100 g
    GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) 0.1 g  in 100 g
    PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) 3 g  in 100 g
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) 0.1 g  in 100 g
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) 13 g  in 100 g
    DIPROPYLENE GLYCOL (UNII: E107L85C40) 3 g  in 100 g
    INVERT SUGAR (UNII: ED959S6ACY) 0.1 g  in 100 g
    SALVIA HISPANICA SEED (UNII: NU0OLX06F8) 0.01 g  in 100 g
    CAPRYLYL GLYCOL (UNII: 00YIU5438U) 0.2 g  in 100 g
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) 0.5643 g  in 100 g
    PROPANEDIOL (UNII: 5965N8W85T) 0.1 g  in 100 g
    1,2-HEXANEDIOL (UNII: TR046Y3K1G) 0.02 g  in 100 g
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) 2 g  in 100 g
    METHICONE (20 CST) (UNII: 6777U11MKT) 0.2084 g  in 100 g
    DIMETHICONE (UNII: 92RU3N3Y1O) 0.2565 g  in 100 g
    GLYCERIN (UNII: PDC6A3C0OX) 2 g  in 100 g
    Product Characteristics
    Colorwhite (Milky White) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76344-8002-21 in 1 BOX12/01/2019
    1NDC:76344-8002-150 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35212/01/2019
    Labeler - Humex,Inc (017945311)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kolmar Korea689512611manufacture(76344-8002)
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