Poison Ivy and Oak Relief

Manufacturer
King Bio Inc.
Effective date
2016-03-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:07:34

Label at a glance#

ProductPoison Ivy and Oak Relief
Active ingredientANACARDIUM OCCIDENTALE FRUIT, CLEMATIS RECTA FLOWERING TOP, CROTON TIGLIUM SEED, CYPRIPEDIUM PARVIFOLUM ROOT, ECHINACEA PURPUREA, ERECHTITES HIERACIIFOLIUS, GRAPHITE, GRINDELIA HIRSUTULA WHOLE, HISTAMINE DIHYDROCHLORIDE, DAPHNE MEZEREUM BARK, TOXICODENDRON PUBESCENS LEAF, URTICA URENS
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts​__________________________________________________________________________________________________________

HPUS active ingredients: Anacardium occidentale, Clematis erecta, Croton tiglium, Cypripedium pubescens, Echinacea purpurea, Erechtites hieracifolia, Graphites, Grindelia, Histaminum hydrochloricum, Mezereum, Rhus toxicodendron, Urtica urens. Equal volumes of each ingredient in 10X, 30X, LM1 potencies.​

INDICATIONS & USAGE SECTION

Uses for temporary relief of skin irritations related to poison ivy, poison oak, poison sumac, detergents, cosmetics, or other irritants: •minor swelling •itching •burning sensation •rashes •skin eruptions with oozing.

† as per various homeopathic materia medicas. These uses have not been evaluated by the FDA, and product has not been clinically tested.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

WARNINGS SECTION

Warnings

  • Stop use and ask a doctor if symptoms persist or worsen.
  • If pregnant or breast-feeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Initially, depress pump until primed.
  • Spray one dose directly into mouth.
  • Adults: 3 sprays 3 times per day.
  • Children ages 2-12: 2 sprays 3 times per day.
  • Use additionally as needed, up to 6 times per day.

OTHER SAFETY INFORMATION

Tamper resistant for your protection. Use only if seal is intact. Keep carton for complete drug facts and product information.

OTC - PURPOSE SECTION

Drug Facts__________________________________________________________________________________________________________

HPUS active ingredients                                           Purpose †

Equal volumes of each ingredient in 10X, 30X, LM1 potencies.

Anacardium occidentale...............................intense itching, swelling

Clematis erecta...........................................red, burning, scaly skin

Croton tiglium........................................severe itching and stinging

Cypripedium pubescens............................................intense itching

Echinacea purpurea..................................................skin irritations

Erechtites hieracifolia............................................red, swollen skin

Graphites.............................................................oozing eruptions

Grindelia................................................severe burning and itching

Histaminum hydrochloricum..................................red, itchy papules

Mezereum.................................................eruption with oozing pus

Rhus toxicodendron........................................intense itching of skin

Urtica urens....................................skin eruptions with burning heat

HPUS indicates the active ingredients are in the official Homeopathic Pharmacopeia of the United States.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-5116-22020-01-31C16284748780-19d75b9d0-a447-f424-e053-dadaa90a57cePoison Ivy and Oak Relief™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-5116-2Poison Ivy and Oak Relief1 in 1 CARTONLIQUID11
57955-5116-2Poison Ivy and Oak Relief59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-5116POISON IVY AND OAK RELIEF (ANACARDIUM OCCIDENTALE, CLEMATIS ERECTA, CROTON TIGLIUM, CYPRIPEDIUM PUBESCENS, ECHINACEA PURPUREA, ERECHTITES HIERACIFOLIA, GRAPHITES, GRINDELIA, HISTAMINUM HYDROCHLORICUM, MEZEREUM, RHUS TOXICODENDRON, URTICA URENS) LIQUID [KING BIO INC.]1Legacy NDC, 2 package rows20160324_4b880ca4-57c2-4a94-8ff6-0979626da049.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-511657955-5116-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

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
610c79f7-8624-465d-87be-8e6edf2f4b474b880ca4-57c2-4a94-8ff6-0979626da0492016-03-24WarningsExact identifier
spl id: 610c79f7-8624-465d-87be-8e6edf2f4b47
spl set id: 4b880ca4-57c2-4a94-8ff6-0979626da049

Reported adverse events (FAERS/openFDA)#

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