FOREST FRESH- triclosan soap

Forest Fresh by

Drug Labeling and Warnings

Forest Fresh by is a Otc medication manufactured, distributed, or labeled by The Dodge Company, Inc., Bayscience Formulators, Bayscience Formulators LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS SECTION

1) For external use only.

2) Do not use in the eyes.

3) Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

Antiseptic handwash for handwashing to decrease baceria on the skin.

OTC - PURPOSE SECTION

Antiseptic handwash

DOSAGE & ADMINISTRATION SECTION

Moisten surface to be cleaned, apply soap, rub to create lather, and rinse.  Repeat as needed.

OTC - ACTIVE INGREDIENT SECTION

Triclosan

INACTIVE INGREDIENT SECTION

cocamidopropyl betaine

cocodiethanolamide

citric acid monohydrate

FD&C blue No.1

imidazolidinyl urea

myristamine oxide

potassium cocoate

propylene glycol

sodium C14-C16 olefin sulfonate

sodium chloride

sodium lauryl sulfate

water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Forest Fresh 8oz.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Forest Fresh 16oz.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Forest Fresh Gal.jpg

INGREDIENTS AND APPEARANCE

FOREST FRESH 
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 25113-222
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.004 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
COCO DIETHANOLAMIDE (UNII: 92005F972D)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
potassium cocoate (UNII: F8U72V8ZXP)
MYRISTAMINE OXIDE (UNII: J086PM3RRT)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
IMIDUREA (UNII: M629807ATL)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 25113-222-85	241 g in 1 BOTTLE
2	NDC: 25113-222-16	482.5 g in 1 BOTTLE
3	NDC: 25113-222-01	3860 g in 1 JUG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/29/2014

Labeler - The Dodge Company, Inc. (001045517)

Registrant - Bayscience Formulators (162935044)

Establishment
Name	Address	ID/FEI	Business Operations
Bayscience Formulators LLC		162930544	manufacture(25113-222)