ACTIVE INGREDIENTS

Oleander 4X
Cicuta virosa 5X
Sulphur 6X
Thuja occidentalis 6X
Medorrhinum 12X
Natrum muriaticum 12X
Psorinum 12X
Syphilinum 12X
Tuberculinum 12X
Vaccinotoxinum 12X

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

For the temporary relief of dry, irritated, red, or itchy skin.*

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

WARNINGS

Consult a doctor if condition worsens or if symptoms persist. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

Keep out of the reach of children.

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

40% ethanol, purified water.

LABEL

Est 1985

Professional Formulas

Complementary Health

Psorinum Combination

Homeopathic Remedy

1 FL. OZ. (29.5 mL)

PSORINUM COMBINATION 9237
psorinum combination liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63083-9237
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
NERIUM OLEANDER WHOLE (UNII: JG9V5H8412) (NERIUM OLEANDER WHOLE - UNII:JG9V5H8412)	NERIUM OLEANDER WHOLE	4 [hp_X] in 29.5 mL
CICUTA VIROSA WHOLE (UNII: 3E698BL84C) (CICUTA VIROSA WHOLE - UNII:3E698BL84C)	CICUTA VIROSA WHOLE	5 [hp_X] in 29.5 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	6 [hp_X] in 29.5 mL
THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (THUJA OCCIDENTALIS LEAF - UNII:0T0DQN8786)	THUJA OCCIDENTALIS LEAF	6 [hp_X] in 29.5 mL
GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F) (GONORRHEAL URETHRAL SECRETION HUMAN - UNII:9BZG9E3I8F)	GONORRHEAL URETHRAL SECRETION HUMAN	12 [hp_X] in 29.5 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	12 [hp_X] in 29.5 mL
SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4) (SCABIES LESION LYSATE (HUMAN) - UNII:5UAU16Z1U4)	SCABIES LESION LYSATE (HUMAN)	12 [hp_X] in 29.5 mL
TREPONEMIC SKIN CANKER HUMAN (UNII: 4ZWP7FWI8W) (TREPONEMIC SKIN CANKER HUMAN - UNII:4ZWP7FWI8W)	TREPONEMIC SKIN CANKER HUMAN	12 [hp_X] in 29.5 mL
BOVINE TUBERCULIN (UNII: HKD62G79N5) (BOVINE TUBERCULIN - UNII:HKD62G79N5)	BOVINE TUBERCULIN	12 [hp_X] in 29.5 mL
VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK) (VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN - UNII:4SV59689SK)	VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN	12 [hp_X] in 29.5 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:63083-9237-1	29.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/15/1985

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		08/15/1984

Labeler - Professional Complementary Health Formulas (167339027)

Registrant - Natural Pharmaceutical Manufacturing LLC (015624923)

Name	Address	ID/FEI	Business Operations
Establishment
Natural Pharmaceutical Manufacturing LLC		015624923	manufacture(63083-9237)

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