BIOXTERMINATE HAND SANITIZER GEL- alcohol gel 
LiquidCapsule Manufacturing LLC

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bioXterminate Hand Sanitizer Gel

Active Ingredient(s)

Alcohol 65% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

  • in children less than 2 months of age
  • on open skin wounds

When using this product keep out of 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 occurs. These may be signs of a serious condition.

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

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

Aloe Vera, carbomer, glycerin, tocopheryl acetate, triethanolamine, deionized purified water.

Package Label

1 Gallon (3785 mL) NDC: 71726-002-06

figure-01

BIOXTERMINATE HAND SANITIZER GEL 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71726-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER 934 (UNII: Z135WT9208)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71726-002-02236.6 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/202010/19/2020
2NDC:71726-002-01118.3 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/202010/19/2020
3NDC:71726-002-03354.9 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/202010/19/2020
4NDC:71726-002-04473.2 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/202010/19/2020
5NDC:71726-002-05946.4 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/202010/19/2020
6NDC:71726-002-063785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/202010/19/2020
7NDC:71726-002-0718927 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/202010/19/2020
8NDC:71726-002-08208198 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/05/202010/19/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/05/202010/19/2020
Labeler - LiquidCapsule Manufacturing LLC (793523890)
Registrant - LiquidCapsule Manufacturing LLC (793523890)
Establishment
NameAddressID/FEIBusiness Operations
LiquidCapsule Manufacturing LLC793523890manufacture(71726-002)

Revised: 12/2023
Document Id: b082f0ef-4056-480e-b6b8-d8cd0b0874fd
Set id: a4e231d1-c1dd-3d3e-e053-2a95a90a1817
Version: 3
Effective Time: 20231222
 
LiquidCapsule Manufacturing LLC