SCYTERA (COAL TAR) FOAM, 2%- coal tar foam, 2% aerosol, foam

Scytera by

Drug Labeling and Warnings

Scytera by is a Otc medication manufactured, distributed, or labeled by DPT Laboratories, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

Scytera™ Foam is an emollient foam containing 10% coal tar topical solution (Liquor Carbonis Detergens) equivalent to 2% coal tar.

Active Ingredient - Purpose

Active ingredient: Coal Tar 2% (from Coal Tar Topical Solution USP, 10%)
Purpose: Psoriasis

Use

For relief of the symptoms of psoriasis.

Warnings

For external use only.

Flammable
Avoid fire, flame, or smoking during and immediately following application.

Do not use

• for prolonged periods without consulting a doctor
• this product in or around the rectum or in the genital area or groin except on the advice of a doctor

Ask a doctor before use if you have

a condition that covers a large area of your body.

Ask a doctor or pharmacist before use if you are

using the product with other forms of psoriasis therapy such as ultraviolet radiation or prescription drugs.

When using this product

• avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
  
• use caution in exposing skin to sunlight after applying this product. It may increase your tendency to sunburn for up to 24 hours after application.
  
• product can stain clothing, contact lenses, and hair. To minimize staining, allow product to dry before contact.
  

Stop use and ask doctor if

condition worsens or does not improve after regular use of this product as directed.

If pregnant or breastfeeding

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away.

Directions

• shake the can well before use.
  
• invert the can to dispense. Upright dispensing will cause loss of propellant.
  
• apply to affected areas one to four times daily or as directed by a doctor.
  

Other information

• contents under pressure. Do not puncture or incinerate.
• store at 68°F to 77°F (20°C to 25°C)
• do not expose to heat or store at temperatures above 120°F (49°C)

Inactive Ingredients

Caprylic/capric triglyceride, ceteareth 20, citric acid, cyclomethicone, dimethicone, EDTA disodium, glycerin, hydroxypropyl methyl cellulose, isopropyl myristate, peppermint oil, phenoxyethanol, potassium sorbate, purified water, sodium citrate, stearic acid, xanthan gum, hydrocarbon (propane/butane) propellant. 

Questions?

1-888-966-8766

WARNINGS

Warning
This product contains chemicals known to the state of California to cause cancer.


Patent Pending
Made in USA.
Marketed by:
Promius Pharma, LLC
Bridgewater, NJ 08807
Under license from
Foamix LTD, Israel

Scytera™ (Coal Tar)Foam 2%, 100 g

Carton and Can Label

NDC: 67857-801-52
Psoriasis Foam

Scytera™
(Coal Tar) Foam 2%

Promius Pharma™
NET WT. 3.3 oz (100 g)

Carton (California)

NDC: 67857-801-26
Psoriasis Foam

Scytera™
(Coal Tar) Foam 2%

Promius Pharma™
NET WT. 3.3 oz (100 g)

Scytera™ (Coal Tar)Foam 2%, 12 g Sample Size

Packer (Box)

Available in 100 g Cans

Scytera™
(Coal Tar) Foam 2%
Promius Pharma™

Professional Samples

Net Quantity 12 x 12 g Cans
NDC: 67857-801-12

Packer (Box) (California)

Available in 100 g Cans

Scytera™
(Coal Tar) Foam 2%
Promius Pharma™

Professional Samples

Net Quantity 12 x 12 g Cans
NDC: 67857-801-19

Can Label

NDC: 67857-801-12
Psoriasis Foam

Scytera™
(Coal Tar) Foam 2%

SAMPLE, NOT FOR SALE
NET WT. 0.4 oz (12 g)

INGREDIENTS AND APPEARANCE

SCYTERA  (COAL TAR) FOAM, 2%
coal tar foam, 2% aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63094-0801
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COAL TAR (UNII: R533ESO2EC) (COAL TAR - UNII:R533ESO2EC)	COAL TAR	20 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSE (UNII: 3NXW29V3WO)
XANTHAN GUM (UNII: TTV12P4NEE)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
STEARIC ACID (UNII: 4ELV7Z65AP)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PEPPERMINT OIL (UNII: AV092KU4JH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63094-0801-1	1 in 1 CARTON
1		100 g in 1 CAN
2	NDC: 63094-0801-2	12 in 1 BOX
2		12 g in 1 CAN
3	NDC: 63094-0801-3	1 in 1 CARTON
3	NDC: 63094-0801-1	100 g in 1 CAN
4	NDC: 63094-0801-4	12 in 1 BOX
4	NDC: 63094-0801-2	12 g in 1 CAN

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358	10/31/2008

Labeler - DPT Laboratories, Ltd. (621782218)