RHUS TOX 6X/12X

Manufacturer
OHM PHARMA INC.
Effective date
2018-10-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:10:31

Label at a glance#

ProductRHUS TOX 6X/12X
Active ingredientTOXICODENDRON PUBESCENS LEAF
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT (HPUS*):

Rhus Toxicodendron 6X/12X

*The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.

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

INDICATIONS & USAGE SECTION

​USES: For Temporary relief of red, swollen, itchy skin.**

DOSAGE & ADMINISTRATION SECTION

​SUGGESTED DOSAGE: ​

3 droppers full 1 time per week for 3 weeks, then 1 time per month thereafter. Hold solution in mouth for 30 seconds then swallow.

Can be taken any time of year but ideal to begin administering during Poision Ivy dormant phase (winter) often starting in February

in the Midwest.

WARNINGS SECTION

​WARNINGS:

If pregnant or nursing, ask a health care professional before using.

Keep out of reach of children. In case of an accidental overdose, seek professional assistance or contact a poison control center immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INACTIVE INGREDIENT SECTION

Alcohol

OTC - QUESTIONS SECTION

QUESTIONS & COMMENTS?

Preckshot Pharmacy / Peoria, IL 61614 / 309-649-2047

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Preckshot Preferred ™

NDC: 66096-745-02

RHUS TOX 6X/12X

HOMEOPATHIC

1 fl oz (30 mL) / Alcohol

RHUS TOX 6X/12XRHUS TOX 6X/12X

OTC - PURPOSE SECTION

For Temporary relief of red, swollen, itchy skin.**

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66096-745-022021-01-29C16284748780-1ba0f9c33-4c64-a910-e053-dadaa90a0b85RHUS TOX 6x/12x

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-745-02RHUS TOX 6X/12X30 mL in 1 BOTTLE, DROPPERLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-745RHUS TOX 6X/12X (RHUS TOXICODENDRON.) LIQUID [OHM PHARMA INC.]1Legacy NDC, 1 package rows20181031_65bdfc5b-9937-4c82-a661-92e8d6193526.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66096-74566096-745-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
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
bc99dddd-922d-4191-879c-fb7627e5c4f765bdfc5b-9937-4c82-a661-92e8d61935262018-10-29WarningsExact identifier
spl id: bc99dddd-922d-4191-879c-fb7627e5c4f7
spl set id: 65bdfc5b-9937-4c82-a661-92e8d6193526

Reported adverse events (FAERS/openFDA)#

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