Label: CORETEX PROFESSIONAL OUTDOOR SKIN PROTECTION WALLET REFILL kit

  • NDC Code(s): 65753-108-39, 65753-109-39, 65753-110-37, 65753-400-39, view more
    65753-515-36
  • Packager: CoreTex Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 4, 2023

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  • Hand Sanitizer Active Ingredients:

    SD Alcohol 40-B 62.5%

  • Hand Sanitizer Purpose

    Antimicrobial

  • Hand Sanitizer Uses:

    Hand Sanitizer to help reduce bacteria on the skin.

  • Hand Sanitizer Warnings

    Flammable. Keep away from heat or flame.

    For external use only.

    When using this product

    do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor

    if irritation or rash appears and lasts.

    Keep out of reach of children. If swallowed, get help or contact a Poison Control Center right away.

  • Hand Sanitizer Directions:

    Put enough product in your palm to cover hands and rub hands together briskly until dry.

  • Hand Sanitizer Inactive Ingredients:

    actinidia chinesis (kiwi) extract, aloe barbadenis leaf juice, aminomethyl propanol, brassica oleracea italica (broccoli) extract, cannabis sativa (hemp) seed extract, carbomer citrullus vulgaris (watermelon) fruit extract, euterpe oleracea fruit extract, fragaria vesca (strawberry) fruit extract, glycerin, helianthus annus (sunfloer) seed oil, hippophae rhamnoides (sea buckthorn) fruit extract, lycium barbarum (goji) extract, myrciaria dubia (camu camu) fruit extract, propanediol, propylene glycol, punica granatum extract, rubus idaeus seed extract, tocopherol acetate (vitamin E acetate), vaccinium angustifolium (blueberry) extract, vaccinium macrocarpon (cranberry) fruit extract, vitis vinifera (grape) seed extra, water

  • Hand Sanitizer Other Information:

    Store below 110 oF (43 o), Read the Safety Data Sheet for this Product. You may obtain an SDS from our website: www.coretexproducts.com or Call: 1-877-684-5774

  • 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

  • SunX 50 Lip Balm Active Ingredients:

    Avobenzone…3.0%

    Homosalate…3.0%

    Octinoxate...7.5%

    Octisalate…5.0%

    Petrolatum...40.0%

  • SunX 50 Lip Balm Purpose

    Sunscreen

    Sunscreen

    Sunscreen

    Sunscreen

    Skin Protectant

  • SunX 50 Lip Balm Uses:

    Helps protect against sunburn and chapped lips.

  • SunX 50 Lip Balm Warnings

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

    Do not use

    Do not use on damaged or broken skin.

    Stop use and ask a doctor if

    • rash occurs

    When using this product

    • keep out of eyes. Rinse to remove.

    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.

  • SunX 50 Lip Balm Directions:

    • Apply liberally before sun exposure and as needed
    • Children under 6 months of age: Ask a doctor before use.
  • SunX 50 Lip Balm Other information:

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

  • SunX 50 Lip Balm Inactive Ingredients:

    C12-15 alkyl benzoate, caprylic/capric triglyceride, mineral oil, ozokerite, phenyl trimethicone, tocopherol.

  • Anti-Itch Active Ingredients:

    Camphor 0.1%

    Diphenhydramine hydrochloride 2%

    Zinc acetate 1%

  • Anti-Itch Purpose

    Extrenal analgesic

    Antihistamine

    Skin protectant

  • Anti-Itch Uses:

    • For the temporary relief of itching and pain associated with minor skin irritations and rashes due to insect bites, poison ivy, poison oak, poison sumac.
    • dries the oozing and weeping of poison ivy, poison oak, poison sumac.
  • Anti-Itch Warnings

    For external use only

    Do Not Use

    • on chicken pox, blisters or on extensive areas of the skin
    • with any drugs containing diphenhydramine while using this product.

    When using this product

    • keep out of eyes.

    Stop use and ask a doctor if

    • conditions worsen or if symptoms 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.

  • Anti-Itch Directions:

    • Adults and children 12 years of age and older, apply to affected area not more than 3 to 4 times daily, or as directed bu a doctor.
  • Anti-Itch Other Information:

    • protect this product from excessive heat and direct sun.
  • Anti-Itch Inactive Ingredients:

    citric acid, diazolidinyl urea, glycerin, hydroxypropyl methylcellulose, methylparaben, propylene glycol, propylparaben, SD alcohol 40, sodium citrate, water (aqua).

  • Anti-Itch 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:

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

  • Sting X Other Information:

    Made in USA for CoreTex Products, Inc.

    Bakersfield, CA 93308

    www.CoreTexProducts.com (877)684-5774

  • Outdoor Professional Kit and Refill Kit Contents

    1 ea – Sun X SPF 30 Broad Spectrum Lotion Pouch

    1 ea – Sun X SPF 30 Broad Spectrum Multi-Pack Pouch w/Towelette
    1 ea – Sun X SPF 30 Lip Balm
    2 ea – Bug X 30 Insect Repellent Towelette
    2 ea – Ivy X Pre-Contact Barrier Towelette
    2 ea – Ivy X Post-Contact Cleanser Towelette
    2 ea – Burn X Lite Cooling Gel Pouch
    1 ea – Anti-Itch Gel Pouch
    1 ea – Sting X Pain Relief Pad
    1 ea – Hand Sanitizer Gel Pouch

  • Professional Outdoor Kit Label

    kit openOutdoor kit

  • Hand Sanitizer Package Label

    65753-200

  • SunX 30 Label

    65753-106

  • SunX 30 Multipack with Towelette Label

    Sunx 30

  • SunX 50 Lip Balm Label

    Lip Balm

  • Anti-Itch Label

    anti itch

  • Sting X Label

    bug x

  • Burn X Label 65753

    Burn X

  • IVY X Cleanser Label

    IVY X Cleanser

  • IVY X Pre Label

    IVY X Pre

  • 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:65753-515
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65753-515-361 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 7 g
    Part 314809258 APPLICATOR 65753105 mL
    Part 41 POUCH 1 mL
    Part 51 POUCH 1.1 mL
    Part 61 POUCH 3.5 mL
    Part 1 of 6
    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 6
    CORETEX SUN X SPF 30 MULTIPACK NEW 
    avobenzone, homosalate, octisalate, octocrylene lotion
    Product Information
    Item Code (Source)NDC:65753-109
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE5 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE7.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)  
    PROPYLENE GLYCOL PROPYL ETHER (UNII: 92KA3PYX0S)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)  
    THEOBROMA CACAO WHOLE (UNII: EB048G1S9J)  
    MEDIUM DENSITY POLYETHYLENE (UNII: 3W404QE89S)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65753-109-397 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/01/2023
    Part 3 of 6
    SUN X SPF 50 BROAD SPECTRUM SUNSCREEN LIP BALM 
    avobenzone, homosalate, octinoxate, octisalate, petrolatum lipstick
    Product Information
    Item Code (Source)NDC:65753-108
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE3 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
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM40 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65753-108-394.44 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/24/2023
    Part 4 of 6
    CORETEX ANTI-ITCH GEL 
    camphor, diphenhydramine, zinc acetate gel
    Product Information
    Item Code (Source)NDC:65753-400
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)0.1 g  in 100 mL
    ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE1 g  in 100 mL
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLCELLULOSE (1500 CPS) (UNII: P0NTE48364)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL 1-ALLYL ETHER (UNII: QRB8092KPK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65753-400-391 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/01/2023
    Part 5 of 6
    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
    Part 6 of 6
    CORETEX ANTIBACTERIAL HAND SANITIZER 
    sd alcohol liquid
    Product Information
    Item Code (Source)NDC:65753-200
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62.5 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    1,3-PROPANEDIOL BIS(4-AMINOBENZOATE) (UNII: 8860R9ORQR)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    13.5 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00411/25/2019
    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(65753-400, 65753-350)
    Establishment
    NameAddressID/FEIBusiness Operations
    CoreTex Products Inc061944620pack(65753-515, 65753-200, 65753-108, 65753-110, 65753-109, 65753-350, 65753-400)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pure Source080354456manufacture(65753-109, 65753-110)
    Establishment
    NameAddressID/FEIBusiness Operations
    Raining Rose083819404manufacture(65753-108)
    Establishment
    NameAddressID/FEIBusiness Operations
    HealthSpecialty794053863manufacture(65753-200)
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