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

Ingredients:

Rhus Toxicodendron 6x/12x

**Claims based on traditional homeopathic practice,

not accepted medical evidence. Not FDA evaluated.

INDICATIONS & USAGE

​Indications: ​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

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.

Keep out of reach of children.

INACTIVE INGREDIENT

Other ingredients: 20% Ethanol

QUESTIONS

​MedCara

126 N. Main

Conrad, IA 50621

(855)-409-5496

www.medcara.com

PRINCIPAL DISPLAY PANEL

NDC: 66096-744-02

Rhus Tox

6x/12x

​CUSTOM ​POISON IVY

HOMEOPATHIC ORAL SOLUTION

1 fl. oz. (30 ml)

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: 66096-744
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: 66096-744-02	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(66096-744)