Hemorrhoidex

Manufacturer
Nartex Laboratorios Homeopaticos SA DE CV
Effective date
2018-02-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:09:16

Label at a glance#

ProductHemorrhoidex
Active ingredientHORSE CHESTNUT, COLLINSONIA CANADENSIS ROOT, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK
Label structure9 sections

Indications and uses

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

Dosage and administration

adults and children over 12 years, take 2 tablets every 6 hours children under 12 years of age, consult a physician

Storage and handling

store in a cool and dry place do not use if box seal is broken or missing

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Aesculus hipp......6C HPUS

Collinsonia...........6C HPUS

Hamamelis..........6C HPUS

Purpose

OTC - PURPOSE SECTION

Aesculus hipp......6C HPUS....................Hemorrhoids, pain after stool, aching, swollen, burning in anus

Collinsonia...........6C HPUS....................Hemorrhoids, itching or burning in anus with swelling

Hamamelis..........6C HPUS.....................Hemorrhoids, pulsation in rectum

The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.  C is a homeopathic dilution: see www.nartexlabusa.com for details.

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you are

  • under a doctor's care for any serious condition
  • taking any other drug

OTC - WHEN USING SECTION

When using this product

  • do not exceed the recommended daily dosage unless directed by a physician

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • symptoms persist, worsen, or if new symptoms occur after 7 days
  • rash develops

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION


  • adults and children over 12 years, take 2 tablets every 6 hours
  • children under 12 years of age, consult a physician

Other information

STORAGE AND HANDLING SECTION


  • store in a cool and dry place
  • do not use if box seal is broken or missing

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Gelatin, Lactose, Magnesium Stearate, Potato Starch, Sodium Benzoate, Talc

Questions or comments?

OTC - QUESTIONS SECTION

1-877-248-1970, between 9am and 5pm PT. informacion@nartexlabs.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hemorrhoidex

Homeopathic Hemorrhoid Tablets

Temporarily relieves discomforting symptoms such as itching, burning, and swelling associated with hemorrhoids

30 Tablets

Hemorrhoidex LabelHemorrhoidex Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
34666-191-12Hemorrhoidex12 in 1 CARTONTABLET126
34666-191-30Hemorrhoidex30 in 1 CARTONTABLET306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
34666-191HEMORRHOIDEX (AESCULUS HIPP, COLLINSONIA, HAMAMELIS) TABLET [NARTEX LABORATORIOS HOMEOPATICOS SA DE CV]6Current NDC, Legacy NDC, 2 package rows20180228_811388f2-d64a-4062-961a-8a2a6ecc1c29.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
COLLINSONIA CANADENSIS ROOTACTIVE INGREDIENTO2630F3XDR1
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKACTIVE INGREDIENTT7S323PKJS1
HORSE CHESTNUTACTIVE INGREDIENT3C18L6RJAZ1
COLLINSONIA CANADENSIS ROOTACTIVE MOIETYO2630F3XDR1
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKACTIVE MOIETYT7S323PKJS1
HORSE CHESTNUTACTIVE MOIETY3C18L6RJAZ1
GELATININACTIVE INGREDIENT2G86QN327L1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I301
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EU1
STARCH, POTATOINACTIVE INGREDIENT8I089SAH3T1
TALCINACTIVE INGREDIENT7SEV7J4R1U1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
34666-19134666-191-30, 34666-191-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 18 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
GELATINGELATIN2G86QN327LTABLET / ORAL46 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUTABLET / ORAL30 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
STARCH, POTATOSTARCH, POTATO8I089SAH3TTABLET / ORAL458 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
GELATINGELATIN2G86QN327LTABLET / ORAL46 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET / ORAL1000 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUTABLET / ORAL30 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUTABLET / ORAL30 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
GELATINGELATIN2G86QN327LTABLET / ORAL46 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET / ORAL1000 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
STARCH, POTATOSTARCH, POTATO8I089SAH3TTABLET / ORAL458 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET / ORAL1000 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
STARCH, POTATOSTARCH, POTATO8I089SAH3TTABLET / ORAL458 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HemorrhoidexAESCULUS HIPP, COLLINSONIA, HAMAMELISNartex Laboratorios Homeopaticos SA DE CV811388f2-d64a-4062-961a-8a2a6ecc1c292018-02-27WarningsExact identifier
ndc (package): 34666-191-12
ndc (package): 34666-191-30
ndc (product): 34666-191
ndc11 (package): 34666019112
ndc11 (package): 34666019130
spl id: 6639326d-58c8-5ffb-e053-2991aa0ab583
spl set id: 811388f2-d64a-4062-961a-8a2a6ecc1c29

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.