POISON IVY/OAK 1013- poison ivy/oak liquid

Poison Ivy/Oak by

Drug Labeling and Warnings

Poison Ivy/Oak by is a Homeopathic medication manufactured, distributed, or labeled by Professional Complementary Health Formulas, Natural Pharmaceutical Manufacturing. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Echinacea purpurea 2X
Adrenal 6X
ACTH 6X, 30X
Liver 6X, 12X
Croton tiglium 8X
Histaminum hydrochloricum 12X
Kreosotum 12X
Xerophyllum 12X
and all the following at 6X, 12X, 60X, 100X:
Rhus diversiloba (poison oak)
Rhus toxicodendron (poison ivy)
Stinging nettle
Sumac

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

For the temporary relief of redness, swelling, stinging, itching of skin, and itching of nose or throat due to sensitivity to poison ivy and poison oak.*

PURPOSE

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

WARNINGS

Severe symptoms such as difficulty breathing, facial swelling, dizziness, confusion, and hives may be life-threatening and require immediate emergency care. 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 to 15 drops up to 3 times per day. For desensitization, begin with 1 to 5 drops daily, increasing to the standard dose gradually to avoid symptom expression; after 1 to 3 months at the standard dose, decrease gradually to a maintenance dose of 10 to 15 drops weekly. 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

20% ethanol, purified water.

LABEL

Est 1985

Professional Formulas

Complementary Health

Poison Ivy/Oak

Homeopathic Remedy

2 FL. OZ. (59 mL)

INGREDIENTS AND APPEARANCE

POISON IVY/OAK  1013
poison ivy/oak liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63083-1013
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ECHINACEA PURPUREA WHOLE (UNII: QI7G114Y98) (ECHINACEA PURPUREA WHOLE - UNII:QI7G114Y98)	ECHINACEA PURPUREA WHOLE	2 [hp_X]  in 59 mL
SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV)	SUS SCROFA ADRENAL GLAND	6 [hp_X]  in 59 mL
CORTICOTROPIN (UNII: K0U68Q2TXA) (CORTICOTROPIN - UNII:K0U68Q2TXA)	CORTICOTROPIN	6 [hp_X]  in 59 mL
BEEF LIVER (UNII: W8N8R55022) (BEEF LIVER - UNII:W8N8R55022)	BEEF LIVER	6 [hp_X]  in 59 mL
CROTON TIGLIUM SEED (UNII: 0HK2GZK66E) (CROTON TIGLIUM SEED - UNII:0HK2GZK66E)	CROTON TIGLIUM SEED	8 [hp_X]  in 59 mL
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	12 [hp_X]  in 59 mL
WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73)	WOOD CREOSOTE	12 [hp_X]  in 59 mL
XEROPHYLLUM ASPHODELOIDES WHOLE (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES WHOLE - UNII:9I4XB1GP2B)	XEROPHYLLUM ASPHODELOIDES WHOLE	12 [hp_X]  in 59 mL
TOXICODENDRON DIVERSILOBUM LEAF (UNII: V727AWD6ZZ) (TOXICODENDRON DIVERSILOBUM LEAF - UNII:V727AWD6ZZ)	TOXICODENDRON DIVERSILOBUM LEAF	6 [hp_X]  in 59 mL
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	6 [hp_X]  in 59 mL
URTICA DIOICA SUBSP. DIOICA LEAF (UNII: 232L6DS3Y4) (URTICA DIOICA SUBSP. DIOICA LEAF - UNII:232L6DS3Y4)	URTICA DIOICA SUBSP. DIOICA LEAF	6 [hp_X]  in 59 mL
AILANTHUS ALTISSIMA FRUIT (UNII: 0W913N2K5N) (AILANTHUS ALTISSIMA FRUIT - UNII:0W913N2K5N)	AILANTHUS ALTISSIMA FRUIT	6 [hp_X]  in 59 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63083-1013-2	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/15/1985

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

Labeler - Professional Complementary Health Formulas (167339027)

Registrant - Natural Pharmaceutical Manufacturing (015624923)

Establishment
Name	Address	ID/FEI	Business Operations
Natural Pharmaceutical Manufacturing		015624923	manufacture(63083-1013)