BAC-D HAND AND WOUND SANITIZER- benzalkonium chloride spray

BAC-D by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial and First aid antiseptic

Uses:

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use. For wound sanitizing to help prevent bacterial contamination in cuts, scrapes, burns, lacerations and skin infections.

Warnings:

For external use only. 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:

Spray hands as needed. Spray wounds 3 times a day after cleaning.

Inactive ingredients:

ionized water, carbamide

SPL UNCLASSIFIED SECTION

DUAL PURPOSE

EXTENDED PROTECTION*

Eliminates 99.99% of Germs

alcohol-free   |    triclosan-free

Non-Irritating Non-Stinging

Antibacterial & Antiseptic

MADE IN THE U.S.A.

Manufactured for

AEC Consumer Products

4525 Campground Road

Fayetteville, NC 28314

www.BAC-D.com

910-987-7964

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

Packaging

INGREDIENTS AND APPEARANCE

BAC-D  HAND AND WOUND SANITIZER
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 86089-400
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: 86089-400-18	18 mL in 1 BOTTLE, SPRAY; 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(86089-400)