RHUS TOX 6X/12X- rhus toxicodendron. liquid

RHUS TOX 6X/12X by

Drug Labeling and Warnings

RHUS TOX 6X/12X by is a Homeopathic medication manufactured, distributed, or labeled by OHM PHARMA INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

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

DOSAGE & ADMINISTRATION

​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

​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.

Keep out of reach of children.

INACTIVE INGREDIENT

Alcohol

QUESTIONS

QUESTIONS & COMMENTS?

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

PRINCIPAL DISPLAY PANEL

Preckshot Preferred ™

NDC: 66096-745-02

RHUS TOX 6X/12X

HOMEOPATHIC

1 fl oz (30 mL) / Alcohol

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

INGREDIENTS AND APPEARANCE

RHUS TOX 6X/12X 
rhus toxicodendron. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66096-745
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	6 [hp_X]  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66096-745-02	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	10/30/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/30/2018

Labeler - OHM PHARMA INC. (030572478)

Registrant - OHM PHARMA INC. (030572478)

Establishment
Name	Address	ID/FEI	Business Operations
OHM PHARMA INC.		030572478	manufacture(66096-745)