DELUXE ALL-PURPOSE- triclosan liquid

DELUXE ALL-PURPOSE by

Drug Labeling and Warnings

DELUXE ALL-PURPOSE by is a Otc medication manufactured, distributed, or labeled by Johnson Labs, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

DELUXE ALL-PURPOSE  
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59854-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	7.57 mL  in 3.78 L

Inactive Ingredients
Ingredient Name	Strength
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
DMDM HYDANTOIN (UNII: BYR0546TOW)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59854-301-01	3.78 L in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2000

Labeler - Johnson Labs, Inc. (805806742)

Registrant - Johnson Labs, Inc. (805806742)

Establishment
Name	Address	ID/FEI	Business Operations
Johnson Labs, Inc.		805806742	manufacture