MUSCLE

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: MUSCLE
Generic name: MENTHOL
Manufacturer: WATER-JEL TECHNOLOGIES
Product type: HUMAN OTC DRUG
SPL set ID: 1af399af-07b0-4899-9bcc-1e244b63b1cf
SPL ID: 32475ac6-c4d4-938d-e063-6294a90a572d
Version: 7
Effective date: 2025-04-08
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:04:43

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 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		MUSCLE	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		WATER-JEL TECHNOLOGIES	openfda.manufacturer_name
ndc	package	59898-805-23	openfda.package_ndc
ndc	package	59898-805-20	openfda.package_ndc
ndc	package	59898-805-05	openfda.package_ndc
ndc	package	59898-805-21	openfda.package_ndc
ndc	package	59898-805-17	openfda.package_ndc
ndc	package	59898-805-25	openfda.package_ndc
ndc	package	59898-805-18	openfda.package_ndc
ndc	package	59898-805-10	openfda.package_ndc
ndc	package	59898-805-24	openfda.package_ndc
ndc	package	59898-805-22	openfda.package_ndc
ndc	product	59898-805	openfda.product_ndc
ndc11	package	59898080518	derived:openfda.package_ndc
ndc11	package	59898080510	derived:openfda.package_ndc
ndc11	package	59898080521	derived:openfda.package_ndc
ndc11	package	59898080522	derived:openfda.package_ndc
ndc11	package	59898080520	derived:openfda.package_ndc
ndc11	package	59898080524	derived:openfda.package_ndc
ndc11	package	59898080523	derived:openfda.package_ndc
ndc11	package	59898080505	derived:openfda.package_ndc
ndc11	package	59898080525	derived:openfda.package_ndc
ndc11	package	59898080517	derived:openfda.package_ndc
rxcui		808955	openfda.rxcui
spl id		32475ac6-c4d4-938d-e063-6294a90a572d	id
spl set id		1af399af-07b0-4899-9bcc-1e244b63b1cf	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 When using this product avoid contact with the eyes do not apply to wounds or damaged skin do not bandage tightly Stop use and ask a doctor if conditions worsens symptoms persist for more than 7 days condition clears up and occurs again within a few days Keep out of the reach of children If swallowed, get medical help or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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