Drug Labeling and Warnings

Drug Details

k">

HAND SANITIZER- benzalkonium chloride solution 
SNYDER MANUFACTURING CORP

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.

----------

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE  0.1%

PURPOSE

ANTIMICROBIAL

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

USES

TO DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE
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 hours.

DIRECTIONS

  • Spray 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, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, citric acid, lavender 4042, eucalyptus 80/85

01b LBL_EuroSpa Hand Sanitizer_2oz

HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73038-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73038-102-1159 mL in 1 BOTTLE; Type 0: Not a Combination Product03/12/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/12/2020
Labeler - SNYDER MANUFACTURING CORP (008277501)

Revised: 3/2020
 
SNYDER MANUFACTURING CORP


© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.