Label: CORETEX PROFESSIONAL OUTDOOR SKIN PROTECTION WALLET REFILL kit

  • NDC Code(s): 65753-110-37, 65753-513-35
  • Packager: CoreTex Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 20, 2023

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  • SunX 30 Active Ingredients:

    Avobenzone 3.0%

    Homosalate 7.5%

    Octisalate 5.0%

    Octocrylene 5.0%

  • SunX 30 Purpose

    Sunscreen

    Sunscreen

    Sunscreen

    Sunscreen

  • SunX 30 Uses:

    • helps prevent sunburn.
    • higher SPF gives more sunburn protection.
    • retains SPF after 80 minutes of activity in the water or sweating.
    • provides high protection against sunburn.
  • SunX 30 Warnings

    For external use only

    SunX 30
    Do Not Use

    • on damaged or broken skin

    When using this product

    • keep out of the eyes
    • rinse with water to remove

    Stop use and ask a doctor if

    • rash or irritation develops and lasts

    Keep out of reach of children.

    If swallowed, get medical help or contact Poison Control Center right away.

  • SunX 30 Directions:

    • apply liberally and evenly 15 minutes before sun exposure
    • reapply:
    • after 80 minutes of swimming or sweating
    • after towel drying, swimming, or
    • at least every 2 hours
    • children under 6 months of age: Ask a doctor
  • SunX 30 Other Information:

    • protect this product from excessive heat or direct sun.

    Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin aging, skin cancer, and other harmful effects of the sun.

  • SunX 30 Inactive Ingredients:

    acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, C12-15 alkyl benzoate, carbomer, disodium EDTA, ethylexyiglycerin, hydroxypropyl methylcellulose, phenoxyethanol, polyethylene, polysorbate 20, propylene glycol, sodium hydroxide, sorbitan oleate, theobroma cacao (cocoa) seed butter, tocopheryl acetate, water

  • SunX 30 Questions?

    Call: 1-877-684-5774

  • Sting X Active Ingredients:

    Benzocaine 6%

  • Sting X Purpose

    Topical Analgesic

  • Sting X Use:

    For temporary pain relief from insect bites and stings

  • Sting X Warnings

    For external use only

    Do not use

    • in or near eyes
    • over large areas of the body
    • over raw or blistered areas

    Stop use and ask a doctor if

    • conditions worsen or persist for more than 7 days or clear up and occur again within a few days

    Keep out of reach of children.

    If swallowed get medical help or contact Poison Control center right away.

  • Sting X Directions:

    Apply to affected area not more than 3 to 4 times daily, for adults and children 2 years of age or older.

  • Sting X Inactive Ingredients:

    allantoin, glycerin, SD alcohol 40, water (aqua)

  • Sting X Other Information:

    Made in USA for CoreTex Products, Inc.

    Erwin, TN 37650

    www.CoreTexProducts.com (877)684-5774

  • Professional Outdoor Kit Label

    CoreTex Hard Kit Label

  • SunX 30 Label 65753-106

    65753-106

  • Sting X

    bug x

  • IVY X Cleanser Label

    Ivy X Cleanser

  • Bug X 30

    Bug X 30

  • Ivy X Solution

    Ivy X Solution

  • INGREDIENTS AND APPEARANCE
    CORETEX PROFESSIONAL OUTDOOR SKIN PROTECTION WALLET REFILL 
    coretex professional outdoor skin protection wallet refill kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65753-513
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65753-513-351 in 1 KIT; Type 0: Not a Combination Product02/24/2023
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 PACKET 44 mL
    Part 21 POUCH 1.1 mL
    Part 1 of 2
    CORETEX SUN X SPF 30 NEW 
    avobenzone, homosalate, octisalate, octocrylene lotion
    Product Information
    Item Code (Source)NDC:65753-110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE7.5 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MEDIUM DENSITY POLYETHYLENE (UNII: 3W404QE89S)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    THEOBROMA CACAO WHOLE (UNII: EB048G1S9J)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)  
    PROPYLENE GLYCOL PROPYL ETHER (UNII: 92KA3PYX0S)  
    Product Characteristics
    Colorwhite (Thick White Lotion) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65753-110-3744 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/01/2023
    Part 2 of 2
    STINGX 
    benzocaine swab
    Product Information
    Item Code (Source)NDC:65753-350
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALLANTOIN (UNII: 344S277G0Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    11.1 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/25/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/24/2023
    Labeler - CoreTex Products Inc (061944620)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosmetic Enterprises017701475manufacture(65753-350)
    Establishment
    NameAddressID/FEIBusiness Operations
    CoreTex Products Inc061944620pack(65753-513, 65753-110, 65753-350)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pure Source080354456manufacture(65753-110)
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