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Rhus tox - Medication Information

Product NDC Code 55714-9020
Drug Name

Rhus tox

Type Generic
Active Ingredients
Toxicodendron pubescens leaf 10 [hp_x]/l
Route ORAL
Dosage Form LIQUID
Labeler Name Newton Laboratories, Inc.
Packages
Package NDC Code Description
55714-9020-6 3 l in 1 jug (55714-9020-6)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
OTC - ACTIVE INGREDIENT SECTION Rhus tox 10x

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
DOSAGE & ADMINISTRATION SECTION Directions: Ages 12 and up, take 6 drops by mouth, (ages 0 to 11, give 3 drops) at bedtime or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENT SECTION Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
INDICATIONS & USAGE SECTION Back strain, pain, and stiffness; pain, soreness and swelling of joints; muscle pain and stiffness.

Purpose

Information about the drug product’s indications for use.
OTC - PURPOSE SECTION Back strain, pain, and stiffness; pain, soreness, and swelling of joints; muscle pain and stiffness.

Spl product data elements

Usually a list of ingredients in a drug product.
Rhus tox Rhus tox WATER ALCOHOL TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL package label

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION Keep out of reach of children.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
QUESTIONS SECTION newtonlabs.net – Questions? 800.448.7256 Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

Pregnancy or breast feeding

Pregnancy or Breast feeding
OTC - PREGNANCY OR BREAST FEEDING SECTION If pregnant or breast-feeding, ask a doctor before use.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
WARNINGS SECTION Warning: Keep out of reach of children. Do not use if tamper - evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API