ALLAPURE ADVANCED FORMULA HAND SANITIZER- benzalkonium chloride liquid 
Allapure, 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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Allapure Advanced Formula Hand Sanitizer

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose

Antiseptic/Hand & Skin Sanitizer

Uses:

Allapure *Advanced Hand Sanitizer & Wound Care is revolutionary wound care and disease protection. It helps decrease bacteria on the skin from cuts, lacerations, incisions and abrasions. Allapure* Advanced Hand Sanitizer & Wound Care promotes healing and is gentle on delicate wound tissue. Recommended for repeated use.

Warnings:

Do not freeze. For external use only.

Do not use

in ears, eyes or mouth.

When using this product, 

avoid contact with the eyes. In case of contact, flush eyes with water.

Stop use and ask a 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 liberally to the palms of the hands or areas of damaged skin. Rub into skin until dry. Repeat if neccesary.

Inactive Ingredients:

1-Octadecyldimethyl(3-Triethoxysilylpropyl) ammonium chloride, Aloe Barbadensis leaf extract, Aqua, C12-C15 Pareth 12, Caprylyl Glucoside, Polyhexanide, Phenoxyethanol, Triethanolamine.

Questions?

+1 877.680.5758, Mon-Fri 9:00AM-5:00PM (PST)

Allapure Advanced Formula Hand Sanitizer 1.7oz (72552-001-01)

Label

Allapure Advanced Formula Hand Sanitizer 7oz (72552-001-07)

Label2

Allapure Advanced Formula Hand Sanitizer 8.25oz (72552-001-08)

Label3

ALLAPURE ADVANCED FORMULA HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72552-001
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
C12-15 PARETH-12 (UNII: 131316X18L)  
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
POLIHEXANIDE (UNII: 322U039GMF)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72552-001-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product09/24/201812/31/2021
2NDC:72552-001-07207 mL in 1 BOTTLE; Type 0: Not a Combination Product09/24/201812/31/2021
3NDC:72552-001-08245 mL in 1 BOTTLE; Type 0: Not a Combination Product09/24/201812/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/24/201812/31/2021
Labeler - Allapure, LLC (081227305)

Revised: 10/2021
Document Id: cdc49bf1-c089-5c5c-e053-2995a90a891f
Set id: 49da284d-0a0e-4efb-89d0-b7cbb66c77eb
Version: 4
Effective Time: 20211007
 
Allapure, LLC