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Rhus Tox by Energique, Inc.

Medically reviewed by Drugs.com. Last updated on Jun 28, 2021.

Dosage form: liquid
Ingredients: TOXICODENDRON PUBESCENS LEAF 200[hp_C] in 1mL
Labeler: Energique, Inc.
NDC Code: 44911-0177

DRUG FACTS:

ACTIVE INGREDIENT:

Rhus Tox 200C.

INDICATIONS:

To be used according to standard homeopathic indications.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional.

Consult a physician for use in children under 12 years of age.

INDICATIONS:

To be used according to standard homeopathic indications.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.


INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol.

QUESTIONS:

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579   800-869-8078

PACKAGE LABEL DISPLAY:

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

RHUS TOX 200C

1 fl. oz. (30 ml)

RHUS TOX 
rhus tox liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0177
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOXICODENDRON PUBESCENS LEAF (TOXICODENDRON PUBESCENS LEAF) TOXICODENDRON PUBESCENS LEAF200 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:44911-0177-130 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/08/2015
Labeler - Energique, Inc. (789886132)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIOperations
Apotheca Company844330915manufacture(44911-0177), api manufacture(44911-0177), label(44911-0177), pack(44911-0177)

 
Energique, Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.