FDA.reportPublic FDA data

Poison Oak Ivy

Manufacturer
Liddell Laboratories, Inc. | Apotheca Company
Effective date
2022-07-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:57:28

Label at a glance#

ProductPoison Oak Ivy
Active ingredientAMANITA MUSCARIA FRUITING BODY, SEMECARPUS ANACARDIUM JUICE, APIS MELLIFERA, CROTON TIGLIUM SEED, CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT, GRINDELIA HIRSUTULA FLOWERING TOP, RANCID BEEF, TOXICODENDRON PUBESCENS LEAF
Label structure9 sections

Dosage and administration

Adults and children over 12: Spray twice under the tongue up to 6 times per day until symptoms are relieved. Children 12 and under: Consult a doctor prior to use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Agaricus Muscarius 6X, Anacardium Orientale 8X, Apis Mellifica 200C, Croton Tiglium 6X, Cypripedium Pubescens 1X, Grindelia 6X, Pyrogenium 30C, Rhus Toxicodendron 6X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with poison oak and poison ivy: inflammation, itching, edema.**

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

WARNINGS:

WARNINGS SECTION

If symptoms persist, consult a doctor.

If pregnant or breast feeding, ask a doctor before use.

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12: Spray twice under the tongue up to 6 times per day until symptoms are relieved.

Children 12 and under: Consult a doctor prior to use.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms associated with poison oak and poison ivy: inflammation, itching, edema.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 20% v/v, Purified water.

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY LIDDELL LABORATORIES INC.

WOODBINE, IA 51579

WWW.LIDDELL.NET  1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS
LIDDELL LABORATORIES

EST. 1994

40POI

Poison Oak + Ivy

HOMEOPATHIC

1.0 FL. OZ. (30 ml)

Poison Oak + IvyPoison Oak + Ivy

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0236-12021-12-21C16284748780-19d75b9d0-10b4-f424-e053-dadaa90a57ceDrug Facts:
50845-0236-12020-01-31C16284748780-19d75b9d0-10b4-f424-e053-dadaa90a57ceDrug Facts:

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-023650845-0236-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMANITA MUSCARIA FRUITING BODYDIF093I037ACTIB
SEMECARPUS ANACARDIUM JUICEY0F0BU8RDUACTIB
APIS MELLIFERA7S82P3R43ZACTIB
CROTON TIGLIUM SEED0HK2GZK66EACTIB
CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT21Y9GZ1LZAACTIB
GRINDELIA HIRSUTULA FLOWERING TOPIDB0NAZ6AIACTIB
RANCID BEEF29SUH5R3HUACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

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
a8d3f26d-5f7f-47ff-8b2e-dd355631ec08d35693d1-b463-49a9-a5bf-6463b527f4ea2022-07-06WarningsExact identifier
spl id: a8d3f26d-5f7f-47ff-8b2e-dd355631ec08
spl set id: d35693d1-b463-49a9-a5bf-6463b527f4ea

Reported adverse events (FAERS/openFDA)#

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