KUB CARTRIDGE REFEEL ANTISEPTIC HAND SANITIZER UNSCENTED- alcohol liquid 
Touchland LLC

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.

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KUB Cartridge Refeel Antiseptic Hand Sanitizer Unscented

Drug Facts

Active Ingredient

Ethyl Alcohol 67%

Purpose

Antiseptic

Uses

  • for handwashing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

For external use only

Flammable, keep away from fire or flame

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 and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

  • place enough product in your palm to thoroughly cover your hands
  • children under 6 years of age should be supervised when using this product
  • rub hands together briskly until dry

Other Information

  • protect the product in this container from excessive heat and direct sun
  • store below 104°F (40°C)
  • may discolor certain fabrics

Inactive ingredients

Water, Aloe Vera Leaf Juice, Radish Root Ferment Filtrate, Glycereth-26, Lime (Citrus Aurantifolia) Seed Oil, Lemon (Citrus Limon) Peel Oil, Limonene.

Package Labeling:

Label0

KUB CARTRIDGE REFEEL ANTISEPTIC HAND SANITIZER UNSCENTED 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72033-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERETH-26 (UNII: NNE56F2N14)  
CITRUS AURANTIIFOLIA SEED OIL (UNII: EW089HAI77)  
LEMON OIL, TERPENELESS (UNII: X69W83NI7V)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72033-010-005 in 1 BOX03/01/201809/30/2021
11000 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/01/201809/30/2021
Labeler - Touchland LLC (036656461)
Establishment
NameAddressID/FEIBusiness Operations
Zobele Mexico S.A. DE C.V.812581940manufacture(72033-010)

Revised: 10/2021
Document Id: cf7f456c-3328-3ee9-e053-2a95a90aae45
Set id: 383345cd-0490-4610-ab42-97f810872942
Version: 3
Effective Time: 20211029
 
Touchland LLC