BAC-D FOAMING WOUND SANITIZER- benzalkonium chloride liquid

BAC-D by

Drug Labeling and Warnings

BAC-D by is a Otc medication manufactured, distributed, or labeled by Great American Emu Company, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

First aid antiseptic

Uses:

• For wound sanitizing to help prevent bacterial contamination in cuts, scrapes, burns, lacerations and skin infections.

Warnings:

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Discontinue use if irritation or redness develops. If condition persists for more than 72 hours consult a doctor.

KEEP OUT OF REACH OF CHILDREN

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

Directions:

Pump onto wounds as needed after cleaning. Allow foam to dissipate. Wipe excess with sterile gauze. May be bandaged once dry.

Inactive ingredients

ionized water, carbamide

SPL UNCLASSIFIED SECTION

KILLS 99.99% OF GERMS

BACTERIAL DEFENSE

EXTENDED PROTECTION*

Benzalkonium Chloride First Aid Antiseptic

Saline-Free

Won't Sting or Irritate

TOUGH ON GERMS

GENTLE ON SKIN

BAC-D Foaming Antibacterial Wound Sanitizer kills bacteria and promotes would healing without stinging. It is safe and effective for cuts, scrapes, burns, lacerations and skin infections, and will not dry, irritate or damage healthy tissue.

Why Saline-Free?

Saline products can over dry skin and trap bacteria in dead skin cells.

BAC-D Technology:

• won't over dry
• won't trap bacteria
• won't stain
• protects longer*

*Studies show Benzalkonium Chloride protects against infection for more than three hours.

MADE IN THE U.S.A.

Manufactured for

AEC Consumer Products

4525 Campground Road

Fayetteville, NC 28314

910-987-7964

www.BAC-D.com

Packaging

INGREDIENTS AND APPEARANCE

BAC-D  FOAMING WOUND SANITIZER
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 86089-300
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 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
UREA (UNII: 8W8T17847W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86089-300-71	210 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2014

Labeler - Great American Emu Company, LLC (080994102)

Establishment
Name	Address	ID/FEI	Business Operations
Great American Emu Company, LLC		080994102	manufacture(86089-300)