MEDICHOICE OB CLEANSING TOWELETTE- benzalkonium chloride liquid

MediChoice OB Cleansing Towelette by

Drug Labeling and Warnings

MediChoice OB Cleansing Towelette by is a Otc medication manufactured, distributed, or labeled by Owens & Minor Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MediChoice OB Cleansing Towelette

Active Ingredient

Benzalkonium Chloride, 0.13%

Purpose

First Aid Antiseptic

Use

First aid antiseptic product to apply topically to the skin to help prevent infection in minor cuts, scrapes, and burns.

Warnings

For external use only.

Do not use

■ in the eyes or apply over large areas of the body.

■ longer than 1 week unless directed by a doctor.

■ on infants Consult a doctor

■ in case of deep or puncture wounds, animal bites, or serious burns.

Stop use and consult a doctor

• if the condition persists or gets worse

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

■Clean the affected area 1 to 3 times daily or as directed by a doctor.

■ May be covered with a sterile bandage when dry.

Other information

• Store at room temperature.
• Allow pad to air dry before disposal.

Inactive Ingredients

Camphor, Propylene Glycol, Purified Water, SD Alcohol 40, Sodium Hydroxide

MediChoice OB Cleansing Towelette 100 Count (

39892-0303-1)

NDC: 39892-0303-1

MEDICHOICE

Cleansing Towelette

Benzalkonium Chloride First Aid Antiseptic

For External use only.

CAUTION: Sterility of contents guaranteed in

unopened, undamaged package.

Not Made with natural latex

sterile

1/Each

Reorder:OB100

Distributed by Owens & Minor

9120 Lockwood Boulevard

Mechanicsville, VA 23116

Made in China

INGREDIENTS AND APPEARANCE

MEDICHOICE OB CLEANSING TOWELETTE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 39892-0303
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 39892-0303-1	100 in 1 BOX	11/11/2014	08/17/2020
1		1600 mg in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/11/2014	08/17/2020

Labeler - Owens & Minor Inc. (847412269)

Registrant - Owens & Minor Inc. (847412269)