DERMAREST  ECZEMA MEDICATED MOIST FOR SENSITIVE SKIN - pramoxine hydrochloride cream 
Insight Pharmaceuticals LLC

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Eczema
MEDICATED
MOISTURIZER
FOR SENSITIVE SKIN

Drug Facts

Active ingredient

Pramoxine hydrochloride 1 %

Purpose

Topical analgesic

Uses

for the temporary relief of pain and itching associated with

Warnings

For external use only

Do not use

When using this product avoid contact with the eyes.

Stop use and ask a doctor if

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

Directions

Other information

Keep carton for full drug facts.

Inactive ingredients

Water, Butylene Glycol, Hamamelis Virginiana (Witch Hazel) Water, Propylene Glycol Dicaprylate/Dicaprate, Cyclopentasiloxane, Myristyl Alcohol, Octyldodecanol, Glyceryl Stearate, PEG-100 Stearate, Polyquaternium-37, Cyclohexasiloxane, Hydrogenated Polyisobutene, Aleurites Moluccana Seed Oil, Tocopheryl Acetate, Zinc PCA, Panthenol, Camellia Sinensis Leaf Extract, Ceramide 3, Chamomilla Recutita (Matricaria) Flower Extract, Aloe Barbadensis Leaf Juice, Allantoin, Ceramide 6 II, Ceramide 1, Phytosphingosine, Cholesterol, Hydroxyphenyl Propamidobenzoic Acid, Sodium Lauroyl Lactylate, Carbomer, Xanthan Gum, Pentylene Glycol, PPG-1 Trideceth-6, Propylene Glycol, Sodium Hydroxide, Disodium EDTA, Caprylyl Glycol, Alcohol, 1,2-Hexanediol

Questions?

call 1-800-344-7239 or visit our website at www.dermarest.com

Distributed by: INSIGHT Pharmaceuticals Corp.
Langhorne, PA 19047-1749

PRINCIPAL DISPLAY PANEL - 56.6g Tube Carton

With
Super Moisturizing
Zinc Complex

DERMAREST®

Eczema

MEDICATED
MOISTURIZER
FOR SENSITIVE SKIN

1% PRAMOXINE
HYDROCHLORIDE
TOPICAL ANALGESIC

24-HOUR
ITCH RELIEF*

Relieves Itching While
It Soothes Dry Skin

Clinically Proven

*when used as directed

DERMAREST
LEADER IN ECZEMA
PSORIASIS RELIEF

NET WT 2oz(56.6g)

PRINCIPAL DISPLAY PANEL - 56.6 g Tube Carton

DERMAREST   ECZEMA MEDICATED MOIST FOR SENSITIVE SKIN
pramoxine hydrochloride   cream
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)63736-325
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Pramoxine Hydrochloride (Pramoxine) Pramoxine Hydrochloride1 g  in 57 g
Inactive Ingredients
Ingredient NameStrength
Water 
Butylene Glycol 
Witch Hazel 
Propylene Glycol Dicaprylate 
Cyclomethicone 5 
Myristyl Alcohol 
Octyldodecanol 
Glyceryl Monostearate 
Polyoxyl 100 Stearate 
Cyclomethicone 6 
.Alpha.-Tocopherol Acetate, D- 
Zinc 
Panthenol 
Green Tea Leaf 
Matricaria Recutita 
Aloe Vera Leaf 
Allantoin 
Xanthan Gum 
Pentylene Glycol 
Propylene Glycol 
Sodium Hydroxide 
Edetate Disodium 
Alcohol 
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
163736-325-2424 CARTON In 1 CASEcontains a CARTON
11 TUBE In 1 CARTONThis package is contained within the CASE (63736-325-24) and contains a TUBE
156.6 g In 1 TUBEThis package is contained within a CARTON and a CASE (63736-325-24)

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34807/23/2010

Labeler - Insight Pharmaceuticals LLC (176792315)
Revised: 07/2010Insight Pharmaceuticals LLC