FDA.reportPublic FDA data

Poison Ivy Dermatosis Drops

Manufacturer
Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing LLC
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:50:10

Label at a glance#

ProductPoison Ivy Dermatosis Drops 2049
Active ingredientECHINACEA PURPUREA WHOLE, GRINDELIA HIRSUTULA FLOWERING TOP, RANUNCULUS BULBOSUS WHOLE, URTICA URENS WHOLE, LYTTA VESICATORIA, DAPHNE MEZEREUM BARK, TOXICODENDRON PUBESCENS LEAF, XEROPHYLLUM ASPHODELOIDES WHOLE, CROTON TIGLIUM SEED
Label structure9 sections

Dosage and administration

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 for up to 6 weeks. For immediate onset of symptoms, take 10 to 15 drops every 15 minutes up to 3 hours. For less severe symptoms, take 10-15 drops hourly up to 8 hours. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Echinacea purpurea 2X
Grindelia 2X
Ranunculus bulbosus 3X
Urtica urens 3X
Cantharis 4X
Mezereum 6X
Rhus toxicodendron 6X
Xerophyllum 6X
Croton tiglium 8X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

Temporarily relieves rashes, blisters, inflammation, or itching of the skin.*

OTC - PURPOSE SECTION

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

WARNINGS

WARNINGS SECTION

Persistent symptoms may be a sign of a serious condition. Consult a doctor immediately if the reaction is severe or widespread, the rash affects the eyes or mouth, or is accompanied by a fever. 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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 for up to 6 weeks. For immediate onset of symptoms, take 10 to 15 drops every 15 minutes up to 3 hours. For less severe symptoms, take 10-15 drops hourly up to 8 hours. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

OTHER SAFETY 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

INACTIVE INGREDIENT SECTION

20% ethanol, purified water.

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est 1985

Professional Formulas

Complementary Health

Poison Ivy Dermatosis Drops

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label imageLabel image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-2049-22026-01-08C16284748780-11030e365-2227-111a-e063-dadaa90a10e2C49
63083-2049-22026-01-08C16284748780-11030e365-2227-111a-e063-dadaa90a10e2C49
63083-2049-22024-01-30C16284748780-11030e365-2227-111a-e063-dadaa90a10e2C49
63083-2049-22024-01-30C16284748780-11030e365-2227-111a-e063-dadaa90a10e2C49

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2049-2Poison Ivy Dermatosis Drops204959 mL in 1 BOTTLE, DROPPERLIQUID592

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-204963083-2049-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ECHINACEA PURPUREA WHOLEQI7G114Y98ACTIB
GRINDELIA HIRSUTULA FLOWERING TOPIDB0NAZ6AIACTIB
RANUNCULUS BULBOSUS WHOLEAEQ8NXJ0MBACTIB
URTICA URENS WHOLEIHN2NQ5OF9ACTIB
LYTTA VESICATORIA3Q034RO3BTACTIB
DAPHNE MEZEREUM BARKX2N6E405GVACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
XEROPHYLLUM ASPHODELOIDES WHOLE9I4XB1GP2BACTIB
CROTON TIGLIUM SEED0HK2GZK66EACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:16:37

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Poison Ivy Dermatosis Drops 2049POISON IVY DERMATOSIS DROPSProfessional Complementary Health Formulasddf4a44f-a919-4bf7-b54d-241ac4c7ffd22026-01-08WarningsExact identifier
ndc (package): 63083-2049-2
ndc (product): 63083-2049
ndc11 (package): 63083204902
spl id: 0add295d-4c20-42ff-96f2-031e177134ae
spl set id: ddf4a44f-a919-4bf7-b54d-241ac4c7ffd2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.