CARROLL ULTREX ANTIMICROBIAL WIPES- benzalkonium chloride cloth 
Carroll Company

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.

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Carroll® Ultrex Antimicrobial Wipes

Drug Facts

Active ingredient

Benzalkonium chloride 0.13% w/w

Purpose

Antimicrobial

Uses

  • for hand cleaning to decrease bacteria on the skin
  • kills 99.9% of most common germs

Warnings

For external use only

When using this product

  • do not use in or near eyes
  • discontinue use if irritation and redness develop

Keep out of reach of children. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

  • Use textured side of wipe to clean hands
  • wet hands thoroughly with product
  • allow to dry without rinsing

Other information

  • store at room temperature

Inactive ingredients

Water, 2-Phenoxyethanol, Alkylpolyglucoside, C 8-10,C10-16, Fragrance, Lauramine,N,N-dimethyl, N-oxide, Tocopherol acetate, Aloe barbadensis leaf juice, PEG-40 Lanolin, Tetrasodium EDTA, Methylchloroisothiazoline, Methylisothiazoline.

Manufactured in the U.S.A. by:
CARROLL® COMPANY
2900 W. Kingsley Rd., Garland, Texas 75041

PRINCIPAL DISPLAY PANEL - 70 Cloth Canister Label

WIPES

CARROLL®

ULTREX
Antimicrobial Wipes

  • Kills 99.9% of common germs
  • Contains Aloe and Vitamin E
  • Moisturizes and conditions skin
  • Alcohol free

CITRUS SCENTED

Dual Textured
Wipe

KEEP OUT OF REACH OF CHILDREN
WARNING
For external use only.

Contains 70
12" x 10" Pre-Moistened Wipes

ITEM #
681

Principal Display Panel - 70 Cloth Canister Label
CARROLL ULTREX ANTIMICROBIAL WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:10685-681
Route of AdministrationPERCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride0.01417 g
Inactive Ingredients
Ingredient NameStrength
Water 
Phenoxyethanol 
Decyl Glucoside 
Lauramine Oxide 
.Alpha.-Tocopherol acetate 
Aloe Vera Leaf 
Edetate Sodium 
Methylchloroisothiazolinone 
Methylisothiazolinone 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10685-681-9770 in 1 CANISTER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E09/15/2012
Labeler - Carroll Company (007372329)

Revised: 9/2012
Document Id: df3d6808-5082-4896-9204-6245ce088205
Set id: d3ab381d-a4ea-43d9-945c-f90c058b1806
Version: 1
Effective Time: 20120908
 
Carroll Company