Hemorrhoidex

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Hemorrhoidex
Generic name: AESCULUS HIPP, COLLINSONIA, HAMAMELIS
Manufacturer: Nartex Laboratorios Homeopaticos SA DE CV
Product type: HUMAN OTC DRUG
SPL set ID: 811388f2-d64a-4062-961a-8a2a6ecc1c29
SPL ID: 6639326d-58c8-5ffb-e053-2991aa0ab583
Version: 6
Effective date: 2018-02-27
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:22

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Hemorrhoidex	openfda.brand_name
generic name		AESCULUS HIPP, COLLINSONIA, HAMAMELIS	openfda.generic_name
manufacturer name		Nartex Laboratorios Homeopaticos SA DE CV	openfda.manufacturer_name
ndc	package	34666-191-12	openfda.package_ndc
ndc	package	34666-191-30	openfda.package_ndc
ndc	product	34666-191	openfda.product_ndc
ndc11	package	34666019112	derived:openfda.package_ndc
ndc11	package	34666019130	derived:openfda.package_ndc
spl id		6639326d-58c8-5ffb-e053-2991aa0ab583	id
spl set id		811388f2-d64a-4062-961a-8a2a6ecc1c29	set_id
unii		O2630F3XDR	openfda.unii
unii		3C18L6RJAZ	openfda.unii
unii		T7S323PKJS	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings 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 do not exceed the recommended daily dosage unless directed by a physician Stop use and ask a doctor if symptoms persist, worsen, 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. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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