CoreTex Professional Outdoor Skin Protection Wallet

Manufacturer
CoreTex Products Inc | Cosmetic Enterprises | Pure Source | Raining Rose | HealthSpecialty
Effective date
2022-11-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:47:06

Label at a glance#

ProductCoreTex Professional Outdoor Skin Protection Wallet
Active ingredientHOMOSALATE, OCTINOXATE, OCTISALATE, AVOBENZONE, OXYBENZONE, OCTOCRYLENE, CAMPHOR (SYNTHETIC), ZINC ACETATE, DIPHENHYDRAMINE HYDROCHLORIDE, BENZOCAINE, ALCOHOL
Label structure52 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on the skin.

Dosage and administration

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

Label contents#

Full prescribing information#

Hand Sanitizer Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

SD Alcohol 40-B 62.5%

Hand Sanitizer Purpose

OTC - PURPOSE SECTION

Antimicrobial

Hand Sanitizer Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Hand Sanitizer Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame.

For external use only.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Hand Sanitizer Directions

DOSAGE & ADMINISTRATION SECTION

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

Hand Sanitizer Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

OTHER SAFETY 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

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 1.0%

Homosalate 5.0%

Octinoxate 7.5%

Octisalate 5.0%

Oxybenzone 6.0%

SunX 30 Purpose

OTC - PURPOSE SECTION

Sunscreen

Sunscreen

Sunscreen

Sunscreen

Sunscreen

SunX 30 Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • If used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun.

SunX 30 Warnings

WARNINGS SECTION

For external use only

SunX 30 Do Not Use

OTC - DO NOT USE SECTION

  • on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash occurs

SunX 30 Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

SunX 30 Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally and evenly 15 minutes before sun exposure
  • Sun Protection Measures: spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and after sun protection measures including:
  • limit time in the sun, especially from 10:00 a.m. - 2 p.m.
  • wear long-sleeved shirts, pants, hats and sunglasses.
  • reapply:
  • after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours
  • children under 6 months of age: Ask a doctor

SunX 30 Other Information

OTHER SAFETY INFORMATION

  • protect this product from excessive heat or direct sun

SunX 30 Inactive Ingredients

INACTIVE INGREDIENT SECTION

acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, butylparaben, calendula officinalis flower extract, carbomer, chamomile recutita extract, dimethicone, dimethyl capramide, ethylparaben, fragrance, glyceryl stearate, isobutylparaben, methylparaben, nasturtium officinale extract, peg-100 stearate, phenoxyethanol, propylparaben, symphytum officinale leaf extract, tetrasodium EDTA, triethanolamine, tocopherol, tocopherol acetate, water

SunX 30 Questions?

OTC - QUESTIONS SECTION

Call: 1-877-684-5774

SunX 30 Lip Balm Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone…3.0%

Homosalate…7.5%

Octisalate…5.0%

Octocrylene…2.5%

Oxybenzone…6.0%

SunX 30 Lip Balm Purpose

OTC - PURPOSE SECTION

Sunscreen

SunX 30 Lip Balm Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

SunX 30 Lip Balm Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash occurs

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. Rinse to remove.

SunX 30 Lip Balm Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

SunX 30 Lip Balm Directions

INDICATIONS & USAGE SECTION

  • apply liberally 15 minutes before sun exposure
  • Use water resistant sunscreen if swimming or sweating
  • Reapply at least every 2 hours
  • Children under 6 months of age: Ask a doctor

SunX 30 Lip Balm Sun Protection Measures

SPL UNCLASSIFIED SECTION

Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures:

  • limit time in the sun, especially from 10a.m.-2p.m.
  • wear long sleeved shirts, pants, hats, and sunglasses.

SunX 30 Lip Balm Inactive Ingredients

INACTIVE INGREDIENT SECTION

Beeswax, castor oil, cocoa butter, coconut oil, shea utter

SunX 30Lip Balm Other information

OTHER SAFETY INFORMATION

Protect this productfrom excessive heat and direct sun.

Anti-Itch Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 0.1%

Diphenhydramine hydrochloride 2%

Zinc acetate 1%

Anti-Itch Purpose

OTC - PURPOSE SECTION

Extrenal analgesic

Antihistamine

Skin protectant

Anti-Itch Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

For external use only

Do Not Use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Anti-Itch Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Anti-Itch Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

OTHER SAFETY INFORMATION

  • protect this product from excessive heat and direct sun.

Anti-Itch Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

Anti-Itch Questions?

OTC - QUESTIONS SECTION

Call: 1-877-684-5774

Sting X Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6%

Sting X Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Sting X Use

INDICATIONS & USAGE SECTION

For temporary pain relief from insect bites and stings

Sting X Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

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

Sting X Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Sting X Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Sting X Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

Sting X Other Information

OTHER SAFETY INFORMATION

Made in USA for CoreTex Products, Inc.

Bakersfield, CA 93308

www.CoreTexProducts.com (877)684-5774

Outdoor Professional Kit and Refill Kit Contents

SPL UNCLASSIFIED SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Professional Outdoor KitProfessional Outdoor Kit

Professional Outdoorkit Refill

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outdoor Kit RefillOutdoor Kit Refill

Hand Sanitizer Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

hand sanitizer labelhand sanitizer label

SunX 30 Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SunX 30SunX 30

SunX 30 Multipack with Towelette Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SunX 30 toweletteSunX 30 towelette

SunX 30 Lip Balm Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lip BalmLip Balm

Anti-Itch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

anti-itch labelanti-itch label

Sting X Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sting X labelSting X label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 80 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 3 · 108 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
23d8e0c2-7979-9289-e063-6394a90aad059b6ff9ca-8d7a-ea1b-e053-2a95a90a514f2024-10-06WarningsExact identifier
spl set id: 9b6ff9ca-8d7a-ea1b-e053-2a95a90a514f
CoreTex Anti-Itch GelCAMPHOR, DIPHENHYDRAMINE, ZINC ACETATECoreTex Products Inc9849da49-d867-fae5-e053-2a95a90a399c2024-10-06WarningsExact identifier
ndc (product): 65753-400
StingXBENZOCAINECoreTex Products Inc98369c97-40f2-13ae-e053-2995a90aaec82023-10-22WarningsExact identifier
ndc (product): 65753-350

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.