Drummond American Trade Wind Antimicrobial

Dosage form: liquid
Ingredients: chloroxylenol 10.22g in 1000mL
Labeler: Lawson Products, Inc.
NDC Code: 62428-505

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.

DRUMMOND AMERICAN TRADE WIND Antimicrobial Lotion Soap

Drug Facts

Active Ingredient

Chloroxylenol (1% v/v)

Purpose

Antiseptic Hand Sanitizer

Uses
  • Helps reduce bacteria that potentially can cause disease
  • Helps prevent cross contamination by hand contact

Warnings
  • For external use only
  • Do not use near eyes
  • Keep out of reach of children.
  • In case of eye contact flush with water for 15 minutes
  • If irritation persists, get medical attention
  • In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions
  • Wet hands and forearms
  • Apply appropriate amount to palm and hand
  • Scrub hands and forearms for 60 seconds
  • Rinse well
  • Wipe dry with towel, repeat if necessary.

Other Information
  • Assists with OSHA bloodborne pathogen standard compliance

Inactive Ingredients

Water, Cocoate, Oleate, Cocamidopropyl betaine, Hydroxyethyl Cellulose, Polyquaternium 7, Na4EDTA, 2-Propanol, Peg-75 Lanolin, Aloe Vera Gel, Fragrance, Triclosan, DMDM Hydantoin.

Principal Display Panel – Bottle Label

DRUMMOND AMERICAN

TRADE WIND

Antimicrobial Lotion Soap

KEEP OUT OF REACH OF CHILDREN

SEE DRUG FACTS PANEL FOR ADDITIONAL INFORMATION.

©Drummond American Corporation 1995 Reproduction in whole or in part prohibited DL3070-0505

Made & printed in U.S.A.

DRUMMOND AMERICAN TRADE WIND ANTIMICROBIAL 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62428-505
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
chloroxylenol (chloroxylenol) chloroxylenol10.22 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
water 
potassium oleate 
cocamidopropyl betaine 
hydroxyethyl cellulose (2000 CPS at 1%) 
isopropyl alcohol 
edetate sodium 
aloe vera leaf 
DMDM hydantoin 
triclosan 
potassium cocoate 
polyquaternium-7 (70/30 acrylamide/DADMAC; 1600 kd) 
Packaging
#Item CodePackage Description
1NDC:62428-505-553785 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33310/28/1998
Labeler - Lawson Products, Inc. (005438890)
Establishment
NameAddressID/FEIOperations
Canberra Corporation068080621MANUFACTURE

Revised: 08/2010
 
Lawson Products, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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