DRUMMOND AMERICAN TRADE WIND ANTIMICROBIAL- chloroxylenol liquid

Drummond American Trade Wind Antimicrobial by

Drug Labeling and Warnings

Drummond American Trade Wind Antimicrobial by is a Otc medication manufactured, distributed, or labeled by Lawson Products, Inc., Canberra Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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.

INGREDIENTS AND APPEARANCE

DRUMMOND AMERICAN TRADE WIND ANTIMICROBIAL 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62428-505
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
chloroxylenol (UNII: 0F32U78V2Q) (chloroxylenol - UNII:0F32U78V2Q)	chloroxylenol	10.22 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
potassium oleate (UNII: 74WHF607EU)
cocamidopropyl betaine (UNII: 5OCF3O11KX)
hydroxyethyl cellulose (2000 CPS at 1%) (UNII: S38J6RZN16)
isopropyl alcohol (UNII: ND2M416302)
edetate sodium (UNII: MP1J8420LU)
aloe vera leaf (UNII: ZY81Z83H0X)
DMDM hydantoin (UNII: BYR0546TOW)
triclosan (UNII: 4NM5039Y5X)
potassium cocoate (UNII: F8U72V8ZXP)
polyquaternium-7 (70/30 acrylamide/DADMAC; 1600 kd) (UNII: 0L414VCS5Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62428-505-55	3785 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	10/28/1998

Labeler - Lawson Products, Inc. (005438890)

Establishment
Name	Address	ID/FEI	Business Operations
Canberra Corporation		068080621	MANUFACTURE