CREW CARE ALCOHOL FREE HAND SANITIZER- benzalkonium chloride liquid 
Quadex LLC

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Crew Care Alcohol Free Hand Sanitizer

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

  • For hand sanitizing to decrease bacteria on the skin 
  • Recommended for repeated use

Warnings

For external use only.

When using this product

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

Stop use and ask a doctor if

irritation or redness develops, or if condition persists for more than 72 hrs.

Keep out of reach of children.

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

Directions

  • Pump a small amount of foam into palm of hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly until dry.

Inactive ingredients

Water, cocamidopropyl PG-dimonium chloride phosphate, dihydroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid, fragrance

Questions?

1-855-WHYIG1 or vortexcompanies.com

Package Labeling: (75254-0305-2)

Bottle4

Package Labeling: (75254-0305-6)

Bottle5

CREW CARE ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75254-0305
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75254-0305-2236 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/202010/31/2023
2NDC:75254-0305-63800 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/202010/31/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)05/01/202010/31/2023
Labeler - Quadex LLC (055544351)

Revised: 1/2024
Document Id: 0e370c3c-c133-ab78-e063-6294a90a2a6a
Set id: a7451f73-8839-13b2-e053-2a95a90a6e79
Version: 3
Effective Time: 20240105
 
Quadex LLC