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

Contacts and useful links#

PhoneLabel contact(855)-409-5496

Websitewww.medcara.com

www.medcara.com

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ingredients:

Rhus Toxicodendron 6x/12x

**Claims based on traditional homeopathic practice,

not accepted medical evidence. Not FDA evaluated.

INDICATIONS & USAGE SECTION

Indications: 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

•If you are 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

Other ingredients: 20% Ethanol

OTC - QUESTIONS SECTION

MedCara

126 N. Main

Conrad, IA 50621

(855)-409-5496

www.medcara.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 66096-744-02

Rhus Tox

6x/12x

CUSTOM POISON IVY

HOMEOPATHIC ORAL SOLUTION

1 fl. oz. (30 ml)

Rhus Tox 6x/12x

OTC - PURPOSE SECTION

For temporary relief of red, swollen, itchy skin.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
66096-744-02	2021-01-29	C162847	48780-1	ba0f9c33-382e-a910-e053-dadaa90a0b85	RHUS TOX 6x/12x

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
66096-744-02	Rhus Tox 6x/12x	30 mL in 1 BOTTLE, DROPPER	LIQUID	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66096-744	RHUS TOX 6X/12X (RHUS TOXICODENDRON.) LIQUID [OHM PHARMA INC.]	1	Legacy NDC, 1 package rows	20181031_7110995e-7520-4c25-8f80-068980aa2dcd.zip

Products#

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

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

Rhus Tox 6x/12x
Rhus Toxicodendron.
TOXICODENDRON PUBESCENS LEAF
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
66096-744	66096-744-02

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
Name	UNII	Kind
TOXICODENDRON PUBESCENS LEAF	6IO182RP7A	ACTIB
ALCOHOL	3K9958V90M	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
732554c8-2c08-4d67-9613-6b4bd08f6eb8			7110995e-7520-4c25-8f80-068980aa2dcd	2018-10-29	Warnings	Exact identifier spl id: 732554c8-2c08-4d67-9613-6b4bd08f6eb8 spl set id: 7110995e-7520-4c25-8f80-068980aa2dcd

Reported adverse events (FAERS/openFDA)#

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