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: HAMAMELIS VIRGINIANA, RATANHIA
Manufacturer: Nartex Laboratorios Homeopaticos, S.A. de C.V.
Product type: HUMAN OTC DRUG
SPL set ID: d469349c-1163-1b5d-e053-2a95a90ae83a
SPL ID: 330fb851-0818-55c2-e063-6294a90ab966
Version: 2
Effective date: 2025-04-18
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:25:39

Harmonized routes table
Harmonized routes
TOPICAL

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Hemorrhoidex	openfda.brand_name
generic name		HAMAMELIS VIRGINIANA, RATANHIA	openfda.generic_name
manufacturer name		Nartex Laboratorios Homeopaticos, S.A. de C.V.	openfda.manufacturer_name
ndc	package	34666-405-01	openfda.package_ndc
ndc	product	34666-405	openfda.product_ndc
ndc11	package	34666040501	derived:openfda.package_ndc
spl id		330fb851-0818-55c2-e063-6294a90ab966	id
spl set id		d469349c-1163-1b5d-e053-2a95a90ae83a	set_id
unii		P29ZH1A35Z	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 For external use only. Do not put this product into rectum by using fingers or any mechanical device or applicator. use if you have an allergy or hypersenstivity to components of the formula or if you have had a prior reaction to this. Stop use and aska doctor if condition worsens. does not improve within 7 days. rash develops. do not exceed the recommended daily dosage unless directed by a doctor. in case of bleeding, consult a doctor promptly. 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.

Reported adverse events (FAERS/openFDA)#

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