FOREST FRESH- triclosan soap 
The Dodge Company, 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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Forest Fresh

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.jpgimage description

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Forest Fresh 16oz.jpgimage description

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Forest Fresh Gal.jpgimage description

FOREST FRESH 
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:25113-222
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.004 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:25113-222-85241 g in 1 BOTTLE
2NDC:25113-222-16482.5 g in 1 BOTTLE
3NDC:25113-222-013860 g in 1 JUG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/29/2014
Labeler - The Dodge Company, Inc. (001045517)
Registrant - Bayscience Formulators (162935044)
Establishment
NameAddressID/FEIBusiness Operations
Bayscience Formulators LLC162930544manufacture(25113-222)

Revised: 4/2014
Document Id: 8c42e75e-3cf4-4ed8-9014-db0fee82a1f7
Set id: 4486715e-3a0a-4b96-bc09-7a45d568dc35
Version: 1
Effective Time: 20140425
 
The Dodge Company, Inc.