ANTIMICROBIAL FACE BODY WASH- benzethonium chloride liquid liquid

ANTIMICROBIAL FACE BODY WASH by

Drug Labeling and Warnings

ANTIMICROBIAL FACE BODY WASH by is a Otc medication manufactured, distributed, or labeled by Bio-Medical & Pharmaceutical Manufacturing Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIMICROBIAL FACE BODY WASH 
benzethonium chloride liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37945-902
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37945-902-08	236 g in 1 BOTTLE; Type 0: Not a Combination Product	10/09/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/09/2015

Labeler - Bio-Medical & Pharmaceutical Manufacturing Corporation (072186356)

Establishment
Name	Address	ID/FEI	Business Operations
Bio-Medical & Pharmaceutical Manufacturing Corporation		072186356	manufacture(37945-902)