PSORIASIS- arsenicum album, arsenicum iodatum, borax, calcarea carbonica, graphites, mezereum, proteus, natrum muriaticum, phytolacca decandra, sepia, silicea, sulphur, thyroidinum liquid

PSORIASIS by

Drug Labeling and Warnings

PSORIASIS by is a Homeopathic medication manufactured, distributed, or labeled by Zorex International, OHM Pharma, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS (*HPUS) - equal amounts of: Arsenicum Album 30C, Arsenicum Iodatum 30C, Borax 30C, Calcarea Carbonica 30C, Graphites 30C, Mezereum 30C, Proteus 30C, Natrum Muriaticum 30C, Phytolacca Decandra 30C, Sepia 30C, Silica 30C, Sulphur 30C, Thyroidinum 30C

PURPOSE

USES: Temporarily relieves rough skin, dry skin eruptions, rose-colored blotches, itchy skin, &/or other symptoms related to psoriasis.**

INDICATIONS & USAGE

USES: Temporarily relieves rough skin, dry skin eruptions, rose-colored blotches, itchy skin, &/or other symptoms related to psoriasis.**

DOSAGE & ADMINISTRATION

DIRECTIONS: Adults and children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF THE REACH OF CHILDREN.  In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

WARNINGS

WARNINGS:

  *Consult a physician for use in children under 12 years of age.

  * IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.

  * KEEP OUT OF THE REACH OF CHILDREN.  In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Inactive Ingredients:  Purified Water, USP Ethanol Alcohol 20%

DO NOT USE

Other Information:  Tamper Seal:  “Sealed for your protection.”   Do not use if seal is broken or missing.

QUESTIONS

Questions & Comments?  Zorex International / Lowell, MI 49331 / 800-679-3027

REFERENCES

*The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

PRINCIPAL DISPLAY PANEL

NDC: 81825-0006-1

PSORIASIS

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

INGREDIENTS AND APPEARANCE

PSORIASIS 
arsenicum album, arsenicum iodatum, borax, calcarea carbonica, graphites, mezereum, proteus, natrum muriaticum, phytolacca decandra, sepia, silicea, sulphur, thyroidinum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81825-0006
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	30 [hp_C]  in 1 mL
SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22)	SODIUM BORATE	30 [hp_C]  in 1 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	30 [hp_C]  in 1 mL
GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O)	GRAPHITE	30 [hp_C]  in 1 mL
DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (DAPHNE MEZEREUM BARK - UNII:X2N6E405GV)	DAPHNE MEZEREUM BARK	30 [hp_C]  in 1 mL
PROTEUS MORGANII (UNII: 56X6LID5ZY) (PROTEUS MORGANII - UNII:56X6LID5ZY)	PROTEUS MORGANII	30 [hp_C]  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	30 [hp_C]  in 1 mL
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG)	PHYTOLACCA AMERICANA ROOT	30 [hp_C]  in 1 mL
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2)	SEPIA OFFICINALIS JUICE	30 [hp_C]  in 1 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	30 [hp_C]  in 1 mL
THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (THYROID, UNSPECIFIED - UNII:0B4FDL9I6P)	THYROID, UNSPECIFIED	30 [hp_C]  in 1 mL
ARSENIC TRIIODIDE (UNII: 3029988O2T) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIIODIDE	30 [hp_C]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81825-0006-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	12/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/01/2021

Labeler - Zorex International (122070786)

Establishment
Name	Address	ID/FEI	Business Operations
OHM Pharma, Inc.		030572478	manufacture(81825-0006)