BAC-D KIDS 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.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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:

For ages 2 years and older. 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

NON-STINGING

Antibacterial

WOUND SANITIZER

Benzalkonium Chloride

Foaming First Aid Antiseptic

EXTENDED PROTECTION*

FOR KIDS!

TOUGH ON GERMS

EASY ON KIDS

Safe & Effective for Use on:

√ Cuts

√ Scrapes

√ Burns

√ Lacerations

√ Skin Infections

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

Made in the U.S.A.

AEC Consumer Products

4525 Campground Road

Fayetteville, NC 28314

910-987-7964

www.BAC-D.com

Packaging

INGREDIENTS AND APPEARANCE

BAC-D  KIDS FOAMING WOUND SANITIZER
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 86089-700
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: 86089-700-17	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2017

Labeler - Great American Emu Company, LLC (080994102)

Establishment
Name	Address	ID/FEI	Business Operations
Great American Emu Company, LLC		080994102	manufacture(86089-700)