Arthcal SOOTHING PAIN RELIEF MASSAGE

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: Arthcal SOOTHING PAIN RELIEF MASSAGE
Generic name: SOOTHING PAIN RELIEF MASSAGE
Manufacturer: Beijing JUNGE Technology Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 3524ad62-0ed6-f2e5-e063-6394a90a3283
SPL ID: 3badf32d-aae8-a2a2-e063-6394a90ad85c
Version: 2
Effective date: 2025-08-06
Source export date: 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:18:04

Harmonized routes table
Harmonized routes
CUTANEOUS

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		M017	openfda.application_number
brand name		Arthcal SOOTHING PAIN RELIEF MASSAGE	openfda.brand_name
generic name		SOOTHING PAIN RELIEF MASSAGE	openfda.generic_name
manufacturer name		Beijing JUNGE Technology Co., Ltd.	openfda.manufacturer_name
ndc	package	85212-0039-1	openfda.package_ndc
ndc	product	85212-0039	openfda.product_ndc
ndc11	package	85212003901	derived:openfda.package_ndc
spl id		3badf32d-aae8-a2a2-e063-6394a90ad85c	id
spl set id		3524ad62-0ed6-f2e5-e063-6394a90a3283	set_id
unii		O80TY208ZW	openfda.unii
unii		856YO1Z64F	openfda.unii
unii		L7T10EIP3A	openfda.unii
unii		344821WD61	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

For external use only Do not apply to wounds or damaged skin Do not bandage tightly .Avoid contact with eyes Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately. lf condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within afew days, discontinue use of this product and consult a physician lf pregnant or breast feeding, ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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