DERMOSCRIBE PSORIASIS- liquor carbonis detergens, salicylic acid cream

DERMOSCRIBE PSORIASIS by

Drug Labeling and Warnings

DERMOSCRIBE PSORIASIS by is a Otc medication manufactured, distributed, or labeled by DERMOSCRIBE PTY LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

LIQUOR CARBONIS DETERGENS 5%, Salicylic Acid 3%

PURPOSE

TREATMENT OF PSORIASIS.

USE

Dermoscribe's Psoriasis Cream is a topical treatment for relief of Psoriasis.

WARNINGS

FOR EXTERNAL USE ONLY. 

Seek medical advice before using if pregnant or breastfeeding. If irritation
develops, stop using and seek medical advice. May not be as effective after expiry date.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

DIRECTIONS

For use only by persons over 12 years old. Apply in a thin layer over the affected area once or twice daily as required.

Use only in accordance with the directions on the label and within the packaging. Refer to enclosed leaflet for detailed directions.

INACTIVE INGREDIENTS

AQUEOUS CREAM

OTHER SAFETY INFORMATION

STORE AT ROOM TEMPERATURE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMOSCRIBE PSORIASIS 
liquor carbonis detergens, salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69683-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COAL TAR (UNII: R533ESO2EC) (COAL TAR - UNII:R533ESO2EC)	COAL TAR	5 g  in 100 g
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
MINERAL OIL (UNII: T5L8T28FGP)
GLYCOL STEARATE (UNII: 0324G66D0E)
SORBITOL (UNII: 506T60A25R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERIN (UNII: PDC6A3C0OX)
COCONUT OIL (UNII: Q9L0O73W7L)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69683-201-11	60 g in 1 BOTTLE; Type 0: Not a Combination Product	02/21/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	02/21/2016

Labeler - DERMOSCRIBE PTY LTD (742164734)