Ma Ying Long Musk Hemorrhoids

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: Ma Ying Long Musk Hemorrhoids
Generic name: PETROLATUM, ZINC OXIDE
Manufacturer: Mayinglong Pharmaceutical Group Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: af466f21-c4bc-3b89-e053-2995a90a49f2
SPL ID: 570bace7-35e4-69bd-e063-6394a90a3f7d
Version: 10
Effective date: 2026-07-20
Source export date: 2026-10-27
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/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:51:30

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Ma Ying Long Musk Hemorrhoids	openfda.brand_name
generic name		PETROLATUM, ZINC OXIDE	openfda.generic_name
manufacturer name		Mayinglong Pharmaceutical Group Co., Ltd.	openfda.manufacturer_name
ndc	package	68511-997-01	openfda.package_ndc
ndc	package	68511-997-20	openfda.package_ndc
ndc	package	68511-997-02	openfda.package_ndc
ndc	product	68511-997	openfda.product_ndc
ndc11	package	68511099720	derived:openfda.package_ndc
ndc11	package	68511099701	derived:openfda.package_ndc
ndc11	package	68511099702	derived:openfda.package_ndc
rxcui		2396041	openfda.rxcui
spl id		570bace7-35e4-69bd-e063-6394a90a3f7d	id
spl set id		af466f21-c4bc-3b89-e053-2995a90a49f2	set_id
unii		4T6H12BN9U	openfda.unii
unii		SOI2LOH54Z	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 and/or intrarectal use only Do not use If allergic to any of the ingredients When using this product Do not exceed the recommended number of daily uses unless directed by a doctor. Do not use the product with an applicator if the introduction of the applicator into the rectum causes additional pain. Consult a doctor promptly. Stop use and ask a doctor if Bleeding occurs Condition worsens or does not improve within 7 days Do not use during pregnancy or when breast-feeding, Consult a health professional before use. Keep out of reach of children to avoid accidental poisoning. If swallowed, get medical help or contact a Poison Control Center right away. Do not use otherwise than as directed.

Reported adverse events (FAERS/openFDA)#

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