MYCO Clinic Pain Relief

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: MYCO Clinic Pain Relief
Generic name: CAMPHOR, MENTHOL
Manufacturer: Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
Product type: HUMAN OTC DRUG
SPL set ID: 0b489420-3b5c-43c5-aab4-0e3720acf9ce
SPL ID: 2763ad7a-a59e-d535-e063-6294a90a7a2d
Version: 2
Effective date: 2024-11-20
Source export date: 2026-10-30
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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:26:48

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		MYCO Clinic Pain Relief	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	openfda.manufacturer_name
ndc	package	24909-013-20	openfda.package_ndc
ndc	package	24909-013-18	openfda.package_ndc
ndc	package	24909-013-50	openfda.package_ndc
ndc	package	24909-013-17	openfda.package_ndc
ndc	product	24909-013	openfda.product_ndc
ndc11	package	24909001318	derived:openfda.package_ndc
ndc11	package	24909001350	derived:openfda.package_ndc
ndc11	package	24909001320	derived:openfda.package_ndc
ndc11	package	24909001317	derived:openfda.package_ndc
rxcui		1802734	openfda.rxcui
spl id		2763ad7a-a59e-d535-e063-6294a90a7a2d	id
spl set id		0b489420-3b5c-43c5-aab4-0e3720acf9ce	set_id
unii		L7T10EIP3A	openfda.unii
unii		N20HL7Q941	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 use on wounds or damaged skin When using this product avoid contact with eyes or mucous membranes - do not bandage tightly or use with a heating pad Stop use and ask a doctor if condition worsens, symptoms persist for more than 7 days, symptoms clear up and occur again within a few days, excessive skin irritation develops If pregnant or breastfeeding , ask a health professional before use. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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