BIOARMOR ALCOHOL FREE HAND SANITIZER- benzalkonium chloride liquid 
BioArmor, 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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BioArmor Alcohol Free Hand Sanitizer

Active Ingredients

Benzalkonium chloride 0.13%

Purpose

Antiseptic Hand Sanitizer   

Uses

  • Hand Sanitizer to help decrease bacteria on skin.
  • Recommended for repeated use.

Warnings

For external use only.

  • Do not use in ears or mouth.

When using this product

  • Avoid contact with eyes.
  • in case of contact flush eyes with water.

Stop use and ask doctor

if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

children should be supervised when using this product.

Directions

Apply a small amount into palms of hands and spread on both hands. Rub into skin until dry.

Inactive Ingredients

1-Octadecanaminium-N,N-dimethyl-N-{3-(trimethoxysilyl)propyl} chloride, Aloe Barbadenis leaf extract, C12-C15 Pareth 12, Caprylyl Glucoside, Citric Acid Monohydrate, Citronellol, FD&C Blue 1, Glycerin, Polyaminopropyl biguanide, Sodium benzoate, Water.

Bioarmor Alcohol-free Hand Sanitizer-50mL

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Bioarmor Alcohol-free Hand Sanitizer-210mL

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BIOARMOR ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70953-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: IQ36O85WQ4)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
C12-15 PARETH-12 (UNII: 131316X18L)  
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70953-001-00210 mL in 1 BOTTLE; Type 0: Not a Combination Product09/06/201612/31/2021
2NDC:70953-001-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product09/06/201612/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/06/201612/31/2021
Labeler - BioArmor, LLC (079341809)
Registrant - BioArmor, LLC (079341809)

Revised: 10/2021
 
BioArmor, LLC