BEIS CLEAN KIT- alcohol 
Beis 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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BEIS Clean Kit

Drug Facts

Active Ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Uses

Warnings

For external use only

Flammable, Keep away from heat or flame

When using this product

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

Stop use and ask a doctor

if irritation or rash appears on the skin.

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

Water, Glycerin, Squalane, Panthenol, Inulin, Sodium Hyaluronate, Fructose, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol.

Drug Facts

Active Ingredient

Ethyl alcohol 75%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only

Flammable, keep away from fire or flame.

Do not use

  • in the eyes

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

wet hands thoroughly with wipe and allow to dry without wiping

Inactive Ingredients

Purified water

Package Labeling:81263-001-00

Label

Package Labeling:81263-002-00

Bottle

BEIS CLEAN KIT 
alcohol kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81263-003
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81263-003-011 in 1 KIT08/01/2021
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 60 mL
Part 210 PATCH 40 mL
Part 1 of 2
BEIS ADVANCED HAND SANITIZER 
alcohol gel
Product Information
Item Code (Source)NDC:81263-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SQUALANE (UNII: GW89575KF9)  
PANTHENOL (UNII: WV9CM0O67Z)  
INULIN (UNII: JOS53KRJ01)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
FRUCTOSE (UNII: 6YSS42VSEV)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81263-001-0060 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 finalpart333E08/01/2021
Part 2 of 2
BEIS HOT MESS ANTIBACTERIAL WIPES 
alcohol cloth
Product Information
Item Code (Source)NDC:81263-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81263-002-0010 in 1 PACKET
14 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/01/2021
Labeler - Beis LLC (117648333)

Revised: 11/2021
Document Id: d178bc61-a1d8-223d-e053-2995a90a08c9
Set id: b7db5a16-c57c-4881-9a9f-f8adaff5424a
Version: 3
Effective Time: 20211123
 
Beis LLC