RHUS TOX 6X/12X- rhus toxicodendron. liquid 
OHM PHARMA INC.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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RHUS TOX 6x/12x

Ingredients:

Rhus Toxicodendron 6x/12x

**Claims based on traditional homeopathic practice,

not accepted medical evidence. Not FDA evaluated.

​Indications: ​For temporary relief of red, swollen, itchy skin.

​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.

•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.

Other ingredients: 20% Ethanol

​MedCara

126 N. Main

Conrad, IA 50621

(855)-409-5496

www.medcara.com

NDC: 66096-744-02

Rhus Tox

6x/12x

​CUSTOM ​POISON IVY

HOMEOPATHIC ORAL SOLUTION

1 fl. oz. (30 ml)

Rhus Tox 6x/12x

For temporary relief of red, swollen, itchy skin.

RHUS TOX 6X/12X 
rhus toxicodendron. liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66096-744
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF6 [hp_X]  in 30 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66096-744-0230 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product10/30/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic10/30/2018
Labeler - OHM PHARMA INC. (030572478)
Registrant - OHM PHARMA INC. (030572478)
Establishment
NameAddressID/FEIBusiness Operations
OHM PHARMA INC.030572478manufacture(66096-744)

Revised: 10/2018
Document Id: 732554c8-2c08-4d67-9613-6b4bd08f6eb8
Set id: 7110995e-7520-4c25-8f80-068980aa2dcd
Version: 1
Effective Time: 20181029
 
OHM PHARMA INC.