Home FDA labels a515d3ae-7a24-45b9-9bcf-a3ec565cd89c Hemorrhoid Gel 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 Hemorrhoid Gel
Generic name ACHILLEA MILLEFOLIUM, AESCULUS HIPPOCASTANUM, HAMAMELIS VIRGINIANA, RUSCUS ACULEATUS, ALOE SOCOTRINA, PAEONIA OFFICINALIS, IGNATIA AMARA, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORUS, PODOPHYLLUM PEITATUM, PULSATILLA, RATANHIA, CHELIDONIUM MAJUS, SULPHUR
Manufacturer Natural Creations, Inc
Product type HUMAN OTC DRUG
SPL set ID d2016513-9b47-490d-9396-766db4cafecd
SPL ID a515d3ae-7a24-45b9-9bcf-a3ec565cd89c
Version 1
Effective date 2018-12-21
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:19:34 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Hemorrhoid Gel openfda.brand_name generic name ACHILLEA MILLEFOLIUM, AESCULUS HIPPOCASTANUM, HAMAMELIS VIRGINIANA, RUSCUS ACULEATUS, ALOE SOCOTRINA, PAEONIA OFFICINALIS, IGNATIA AMARA, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORUS, PODOPHYLLUM PEITATUM, PULSATILLA, RATANHIA, CHELIDONIUM MAJUS, SULPHUR openfda.generic_name manufacturer name Natural Creations, Inc openfda.manufacturer_name ndc package 43406-0709-5 openfda.package_ndc ndc product 43406-0709 openfda.product_ndc ndc11 package 43406070905 derived:openfda.package_ndc spl id a515d3ae-7a24-45b9-9bcf-a3ec565cd89c id spl set id d2016513-9b47-490d-9396-766db4cafecd set_id unii 27YLU75U4W openfda.unii unii 2FXJ6SW4PK openfda.unii unii 7E889U5RNN openfda.unii unii 269XH13919 openfda.unii unii 2S713A4VP3 openfda.unii unii 8R564U2E1P openfda.unii unii 411VRN1TV4 openfda.unii unii 3C18L6RJAZ openfda.unii unii 1NM3M2487K openfda.unii unii V5VD430YW9 openfda.unii unii P29ZH1A35Z openfda.unii unii 70FD1KFU70 openfda.unii unii 5KEZ82GMGU openfda.unii unii I76KB35JEV 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 TOPICAL USE ONLY. Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.