DERMATIZE- benzethonium chloride liquid 
Anderson Chemical Company

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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Active ingredient

Benzethonium chloride, 0.2% w/v

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on skin.

Warning

For external use only.

When using this product

Stop use and ask a doctor if

Stop use and ask a doctor if irritation or redness develops, or if conditions persist for more than 72 hours.

Keep out of reach of children.

Keep out of reach of children, except under adult supervision.

Directions

Inactive ingredients

Citric acid; 1,3-Dihydroxymethyl-5,5-dimethylhydantoin and 3-iodo-2-propynyl butyl carbamate; Ethoxylated C11 Alcohol; Hydrogenated starch hydrolysate; Hydroxypropyl methylcellulose; N-alkykl (C12-C16)-N, N-dimethylamine oxide; Sodium hydroxide; Water.

Questions or comments?

320-693-2477

Principal Display Panel

Product Label

DERMATIZE 
benzethonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63131-0004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
HYDROXYMETHYL CELLULOSE (UNII: 273FM27VK1)  
COCAMINE OXIDE (UNII: QWA2IZI6FI)  
HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)  
UNDECETH-7 (UNII: R6B5PCO2JN)  
WATER (UNII: 059QF0KO0R)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63131-0004-115140 in 1 CASE10/02/2020
13785 mL in 1 JUG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/02/2020
Labeler - Anderson Chemical Company (006179220)
Establishment
NameAddressID/FEIBusiness Operations
Anderson Chemical Company006179220manufacture(63131-0004)

Revised: 5/2020
Document Id: a501d01d-a400-10aa-e053-2a95a90aa7e0
Set id: a501d01d-a3ff-10aa-e053-2a95a90aa7e0
Version: 1
Effective Time: 20200506
 
Anderson Chemical Company