ANTIMICROBIAL FACE BODY WASH- benzethonium chloride liquid liquid 
Bio-Medical & Pharmaceutical Manufacturing Corporation

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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Drug Facts

Antimicrobial Wash

Active Ingredients

Benzethonium Chloride 0.2%

Purpose

Antimicrobial

Use

A unique, non-drying cleanser.
Developed for all skin types and pH balanced.
Helps to decrease bacteria on the skin.

Warnings

External use only.
Do not use in eyes.
In case of deep wounds or puncture wounds, consult a physician.
If irritation develops and persists for more than a few days, discontinue use and consult a physician.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately. (1-800-222-1222)

Directions

Wet hands and other areas to be treated.
Place a small amount of gel in your hands and work into lather.
Apply lather to areas to be treated using a gentle, circular motion.

Rinse clean.

Other information

Alcohol Free

Moisturizes

Made In USA

Inactive Ingredients

Purified Water, Ammonium Lauryl Sulfate, Lauramidopropyl Betaine, Hydroxypropyl Bis- Hydroxyethyldimonium Chloride, Propylene Glycol, Hydroxypropylmethylcellulose, Sodium Chloride, Diazolidinyl Urea, PEG-4 Laurate, Methylparaben, Propylparaben, 3-iodo-2-propynylbutylcarbamate.

Questions or Comments

Bio-Medical & Pharm. Mfg. Corp.

4311 South Dr.,

Houston, TX 77053-4820

Phone: 281.835.8051

Label

ANTIMICROBIAL FACE BODY WASH 
benzethonium chloride liquid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37945-902
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)  
PEG-4 LAURATE (UNII: AYF4VM3N1Z)  
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
HYDROXYPROPYL BIS-HYDROXYETHYLDIMONIUM CHLORIDE (UNII: 1EO3O1X7HG)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37945-902-08236 g in 1 BOTTLE; Type 0: Not a Combination Product10/09/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/09/2015
Labeler - Bio-Medical & Pharmaceutical Manufacturing Corporation (072186356)
Establishment
NameAddressID/FEIBusiness Operations
Bio-Medical & Pharmaceutical Manufacturing Corporation072186356manufacture(37945-902)

Revised: 4/2020
Document Id: a346ebd2-fc2e-b574-e053-2995a90a0d3a
Set id: 210dc091-4a9b-0c48-e054-00144ff88e88
Version: 5
Effective Time: 20200415
 
Bio-Medical & Pharmaceutical Manufacturing Corporation