HIONFURT Motion Sickness

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: HIONFURT Motion Sickness
Generic name: MOTION SICKNESS NATURAL HERBAL PLANT
Manufacturer: Puning Huiyu E-Commerce Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 2e2c9073-1dcf-a3e8-e063-6394a90a6ee3
SPL ID: 2e2c9073-1dd0-a3e8-e063-6394a90a6ee3
Version: 1
Effective date: 2025-02-15
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/3744b3ae389d13e8f30cade845ea29e0fc75bb043dcda980c2025693f0c10522/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 09:09:44

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M009	openfda.application_number
brand name		HIONFURT Motion Sickness	openfda.brand_name
generic name		MOTION SICKNESS NATURAL HERBAL PLANT	openfda.generic_name
manufacturer name		Puning Huiyu E-Commerce Co., Ltd.	openfda.manufacturer_name
ndc	package	85213-003-01	openfda.package_ndc
ndc	package	85213-003-05	openfda.package_ndc
ndc	package	85213-003-03	openfda.package_ndc
ndc	package	85213-003-04	openfda.package_ndc
ndc	package	85213-003-02	openfda.package_ndc
ndc	product	85213-003	openfda.product_ndc
ndc11	package	85213000303	derived:openfda.package_ndc
ndc11	package	85213000302	derived:openfda.package_ndc
ndc11	package	85213000304	derived:openfda.package_ndc
ndc11	package	85213000301	derived:openfda.package_ndc
ndc11	package	85213000305	derived:openfda.package_ndc
spl id		2e2c9073-1dd0-a3e8-e063-6394a90a6ee3	id
spl set id		2e2c9073-1dcf-a3e8-e063-6394a90a6ee3	set_id
unii		213N3S8275	openfda.unii
unii		WW64GZ6LQY	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

warning Pregnant women, breastfeeding mothers, children under the age of 4 should not use .Do not use if the skin has abnormalities, wounds, eczema, inflammation, allergies. Please keep it out of reach of children and pets. For external use only.

Reported adverse events (FAERS/openFDA)#

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