Rhus Tox 4X, 8X, 12X

Manufacturer
OHM PHARMA INC.
Effective date
2018-01-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:11

Label at a glance#

ProductRhus Tox 4X, 8X, 12X
Active ingredientTOXICODENDRON PUBESCENS LEAF
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*):

Rhus Toxicodendron 4X, 8X, 12X (Relieves Poison Ivy & Posion Oak).

INDICATIONS & USAGE SECTION

USES: Temporarily relieves intense itching & skin irritation from contact with Poison Ivy & /or Poison Oak.

OTC - PURPOSE SECTION

(Relieves Poison Ivy & Poison Oak)

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Best taken between meals. Mint flavored foods (mouthwash, mints, etc.) should be avoided. When taking the 3 droppers, the solution should be held in the mouth for 30 seconds then swallowed. Repeat the dose on the same day weekly for three consectutive weeks.

WARNINGS SECTION

WARNINGS:

Consult a physician for use in children under 12 years of age.

IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water.

OTC - QUESTIONS SECTION

QUESTIONS & COMMENTS?:

MFG FOR: Village Pharmacy / 2541 East Broadway, Maryville, TN 37804

PH: (865) 983-9590  /  www.villagepharmacy.biz

OTHER SAFETY INFORMATION

​OTHER INFORMATION: ​Tamper Seal; "Sealed for your protection".

Do not use if seal is broken or missing.

*The letters "HPUS" indicater that the components in this product are officially monographed in the Homeopathic

Pharmacopeiaof the United States.

** Claims based on traditional homeoplathic practice, not accepted medical evidence. Not FDA eveluated.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Village Pharmacy

NDC: 66096-731-02

RHUS TOX

ORAL SOLUTION

4X, 8X, 12X

Poison Ivy * Poison Oak

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

1 fl. oz. bottle label1 fl. oz. bottle label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66096-731-022021-01-29C16284748780-1ba0f9c33-4164-a910-e053-dadaa90a0b85RHUS TOX 4X, 8X, 12X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-731-02Rhus Tox 4X, 8X, 12X30 mL in 1 BOTTLE, DROPPERLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-731RHUS TOX 4X, 8X, 12X (RHUS TOXICODENDRON.) LIQUID [OHM PHARMA INC.]1Legacy NDC, 1 package rows20180129_e7fa5ff6-b4f8-4581-beb0-d07cb9c1f028.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66096-73166096-731-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
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
0667f0bc-7e7f-4e12-a153-78f5b598f208e7fa5ff6-b4f8-4581-beb0-d07cb9c1f0282018-01-19WarningsExact identifier
spl id: 0667f0bc-7e7f-4e12-a153-78f5b598f208
spl set id: e7fa5ff6-b4f8-4581-beb0-d07cb9c1f028

Reported adverse events (FAERS/openFDA)#

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