BAC-D HAND AND WOUND SANITIZER- benzalkonium chloride spray 
AEC CONSUMER PRODUCTS

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

BAC-D Hand and Wound Sanitizer

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. 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

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

image description

BAC-D  HAND AND WOUND SANITIZER
benzalkonium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:86089-400
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
UREA (UNII: 8W8T17847W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:86089-400-1818 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/01/201404/01/2020
2NDC:86089-400-0259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2014
Labeler - AEC CONSUMER PRODUCTS (080994102)
Establishment
NameAddressID/FEIBusiness Operations
AEC CONSUMER PRODUCTS080994102manufacture(86089-400) , pack(86089-400)
Establishment
NameAddressID/FEIBusiness Operations
Holly Oak Chemical, Inc.057840035manufacture(86089-400)
Establishment
NameAddressID/FEIBusiness Operations
Cosco International, Inc.016433141pack(86089-400)

Revised: 1/2022
Document Id: 97245535-f475-4170-b03a-4f03b7690fa1
Set id: 51347d59-c0eb-4695-ba6e-46042f62110a
Version: 5
Effective Time: 20220103
 
AEC CONSUMER PRODUCTS