Topical Hemorrhoid Relief 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: Topical Hemorrhoid Relief Gel
Generic name: MENTHOL, UNSPECIFIED FORM
Manufacturer: Yantai Aien Biotechnology Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 4d6e6667-ab1c-de7c-e063-6294a90a0b9b
SPL ID: 4d6e6667-ab1d-de7c-e063-6294a90a0b9b
Version: 1
Effective date: 2026-03-20
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:58:21

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Topical Hemorrhoid Relief Gel	openfda.brand_name
generic name		MENTHOL, UNSPECIFIED FORM	openfda.generic_name
manufacturer name		Yantai Aien Biotechnology Co., Ltd.	openfda.manufacturer_name
ndc	package	87512-005-01	openfda.package_ndc
ndc	package	87512-005-02	openfda.package_ndc
ndc	product	87512-005	openfda.product_ndc
ndc11	package	87512000502	derived:openfda.package_ndc
ndc11	package	87512000501	derived:openfda.package_ndc
rxcui		2739217	openfda.rxcui
spl id		4d6e6667-ab1d-de7c-e063-6294a90a0b9b	id
spl set id		4d6e6667-ab1c-de7c-e063-6294a90a0b9b	set_id
unii		L7T10EIP3A	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 useI If you are allergic to menthol orany other ingredient in this product When using this productAvoid contact with eyes. Ifcontact occurs, rinse thoroughly with waterDo not put this product into therectum by using fingers or anymechanical device or applicator Stop use and ask a doctor ifCondition worsens or does notimprove within 7 days Bleeding occursRedness, irritation, swelling, pain,or other symptoms develop or increaseAllergic reaction occurs

Reported adverse events (FAERS/openFDA)#

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