Label: RHUS TOX 6X/12X- rhus toxicodendron liquid
- NDC Code(s): 82406-0001-1
- Packager: MedCara Pharmaceuticals, LLC
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated March 3, 2022
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- PURPOSE
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DOSAGE & ADMINISTRATION
DIRECTIONS: Adults and children above 12 years: 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 at any time of year but ideal to begin administering during Poison Ivy dormant phase (winter) often starting in February in the Midwest.
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
WARNINGS:
- Consult a physician for use in children under 12 years of age.
- IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
- KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
- Do not use if TAMPER EVIDENT seal is broken or missing.
- INACTIVE INGREDIENT
- QUESTIONS
- REFERENCES
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RHUS TOX 6X/12X
rhus toxicodendron liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82406-0001 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 12 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82406-0001-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 02/17/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/17/2022 Labeler - MedCara Pharmaceuticals, LLC (966701166) Establishment Name Address ID/FEI Business Operations OHM Pharma, Inc 030572478 manufacture(82406-0001)