CHEMCOR CHEMICAL FOAMING HAND SANITIZER- benzalkonium chloride liquid 
Chemcor Chemical Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Foaming Hand Sanitizer

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

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 hours.

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

Directions

Inactive Ingredients

Water, Cocamidopropyl PG-dimonium Chloride Phosphate, Dihydroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid.

no alcohol

dye and fragrance free

tough on germs and bacteria

CHEMCOR

CHEMICAL CORP

CHINO, CA 91710

CHEMCORCHEMICAL.COM

WARNING

KEEP OUT OF REACH OF CHILDREN.

MAY BE HARMFUL IF SWALLOWED.

MAY CAUSE EYE IRRITATION.

SEE BACK PANEL FOR ADDITIONAL PRECAUTIONS AND FIRST AID.

institutional & commercial hand Sanitizer

Before discarding container, rinse with water.

For institutional and commercial use.

Foaming Hand Sanitizer

image description
CHEMCOR CHEMICAL FOAMING HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68041-519
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0013 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:68041-519-004 in 1 BOX06/01/2020
1NDC:68041-519-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/01/2020
Labeler - Chemcor Chemical Corporation (018129978)
Establishment
NameAddressID/FEIBusiness Operations
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.028311595manufacture(68041-519) , api manufacture(68041-519) , pack(68041-519)

Revised: 12/2023
Document Id: 5d1a6d2d-b64d-4690-9668-d81c887aff29
Set id: 5c9d90c1-0381-4237-9529-398fa51b3ab4
Version: 5
Effective Time: 20231214
 
Chemcor Chemical Corporation