Hemorrhoidex

RATANHIA, HAMAMELIS TOPICAL HUMAN OTC DRUG

Hemorrhoidex is an FDA drug label for the active ingredient RATANHIA, HAMAMELIS manufactured by Nartex Laboratorios Homeopaticos SA DE CV administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20220228.

Generic name
RATANHIA, HAMAMELIS
Manufacturer
Nartex Laboratorios Homeopaticos SA DE CV
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
34666-201
Application
N/A
Label effective
20220228

About this product

Hemorrhoidex is an FDA-registered drug product whose active ingredient is RATANHIA, HAMAMELIS. It is labelled by Nartex Laboratorios Homeopaticos SA DE CV taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 34666-201, label effective 20220228. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing RATANHIA, HAMAMELIS are most often described in connection with: temporarily relieves, discomforting symptoms, itching burning, swelling associated, hemorrhoids product, based homeopathic, materia medica, drug administration. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Ratanhia ........................3X HPUS Hamamelis ....................1X HPUS

Indications & Usage

Uses Temporarily relieves discomforting symptoms such as itching, burning, and swelling associated with hemorrhoids. Product Uses are based on Homeopathic Materia Medica. This product and its Uses have not been evaluated by the Food and Drug Administration. This product has not been clinically tested by Nartex Labs USA, Inc.

Dosage & Administration

Directions adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Apply generously to affected area up to 2 times daily, especially at night, in the morning or after each bowel movement reapply if needed children under 12 years of age, consult a physician

Warnings

Warnings For external use only Do not use if you have an allergy or hypersensitivity to components of the formula or if you have had a prior reaction to this product Ask a doctor before use if you are under a doctor's care for any serious condition taking any other drug When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water do not exceed the recommended daily dosage unless directed by physician Stop use and ask a doctor if bleeding occurs symptoms persist, worse, or if new symptoms occur after 7 days rash develops If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Frequently asked questions

What is Hemorrhoidex used for?
Uses Temporarily relieves discomforting symptoms such as itching, burning, and swelling associated with hemorrhoids. Product Uses are based on Homeopathic Materia Medica. This product and its Uses have not been evaluated by the Food and Drug Administration. This product has not been clinically tested by Nartex Labs USA, Inc.

Who makes Hemorrhoidex?
Nartex Laboratorios Homeopaticos SA DE CV is the labeler of record for Hemorrhoidex.

What form does Hemorrhoidex come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Hemorrhoidex prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Hemorrhoidex been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.