PSORIASIS REAL RELIEF- sulphur, arsenicum album, alumen, magnesia sulphuricum, natrum sulphuricum tablet, chewable

PSORIASIS by

Drug Labeling and Warnings

PSORIASIS by is a Homeopathic medication manufactured, distributed, or labeled by HOMEOLAB USA INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS HPUS

Sulphur (Sublimed sulfur) 8X
Arsenicum album (Arsenous oxide) 8X
Alumen (Potassium alum) 8X
Magnesia sulphurica (Magnesium sulfate) 8X
Natrum sulphuricum (Disodium sulfate) 8X

REFERENCES

The letters 'HPUS' indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

PURPOSE

burning itching peeling dry skin
dry and cracked skin, reddish spots, burning itching (fish-scales), itchy pimples
itching and redness
stinging itching spots on skin
itching pimples (moist and oozing)

USES

This homeopathic medicine helps relieve symptoms of psoriasis:

- dry peeling skin

- stinging

- burning itching

- redness

- itching spots

WARNINGS

Stop use and ask a doctor if symptoms worsen or persist for more than 7 days.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

DIRECTIONS

Chew tablets and let dissolve in mouth.

Do not use more than directed.

Do not take with food.

Repeat 3 times daily and reduce with improvement or as directed by a health professional.

Age	Dose
Adults and children 12 years of age and older	2 tablets
Children 2 to 11 years of age	1 tablet
Children under 2 years of age	Ask a doctor

OTHER INFORMATION

Store at room temperature (68 - 77F).

Do not use if seal is broken or missing.

INACTIVE INGREDIENTS

Lactose, magnesium stearate.

CARTON

INGREDIENTS AND APPEARANCE

PSORIASIS  REAL RELIEF
sulphur, arsenicum album, alumen, magnesia sulphuricum, natrum sulphuricum tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60512-6010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	8 [hp_X]
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC CATION (3+)	8 [hp_X]
POTASSIUM ALUM (UNII: 1L24V9R23S) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0)	ALUMINUM HYDROXIDE	8 [hp_X]
MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM CATION	8 [hp_X]
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750)	SODIUM SULFATE ANHYDROUS	8 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	8mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60512-6010-0	90 in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/11/2012

Labeler - HOMEOLAB USA INC (202032533)

Establishment
Name	Address	ID/FEI	Business Operations
HOMEOLAB USA INC		202032533	manufacture(60512-6010)