DELUXE ALL-PURPOSE  - triclosan liquid 
Johnson Labs, Inc.

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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Active Ingredient

Drug Facts  Active Ingredients  Triclosan 0.2 %

Purpose

Purpose  Handwash

Keep Out of Reach of Children

Keep out of reach of children - If swallowed get medical help or contact a Poison Control Center immediately.

Uses

Antimicrobial handwash.

Warnings

Warnings - For external use only.

When using this product - Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Directions

Directions - Dispense a small amount of soap into hands or on a washcloth. Work up a lather and rinse with water.

Inactive Ingredients

Inactive Ingredients - As-40, Cd-6, Color, Dantogard, Propylene Glycol, Water.

Package Label

Johnson Labs   DELUXE ALL-PURPOSE LIQUID HAND SOAP

This state-of-the-art hand soap was developed to be used in industries, schools, offices or wherever people need a high quality hand soap. This product can also be used as a hair and body shampoo and clothes wash.

1 Gallon (3.78L)  made in U.S.A.  Johnson Labs, Inc. Troy, AL 36081  334-566-9152  800-473-9152

Deluxe All-Purpose Liquide Hand Soap

DELUXE ALL-PURPOSE  
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59854-301
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN7.57 mL  in 3.78 L
Inactive Ingredients
Ingredient NameStrength
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59854-301-013.78 L in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2000
Labeler - Johnson Labs, Inc. (805806742)
Registrant - Johnson Labs, Inc. (805806742)
Establishment
NameAddressID/FEIBusiness Operations
Johnson Labs, Inc.805806742manufacture

Revised: 4/2012
Document Id: d76f4f10-eba1-455e-8568-2291e6fad7ad
Set id: 670f79ff-1647-461e-a612-158ebd5b72fc
Version: 1
Effective Time: 20120402
 
Johnson Labs, Inc.