ORCA Complete Menthol Pain Reliever

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: ORCA Complete Menthol Pain Reliever
Generic name: MENTHOL
Manufacturer: ORCA Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 99990e27-d66b-4d61-97f2-6a76066eb8b8
SPL ID: 0c06e3d2-4481-f4b5-e063-6394a90a0608
Version: 3
Effective date: 2023-12-08
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:23:37

Harmonized routes table
Harmonized routes
ORAL

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		M022	openfda.application_number
brand name		ORCA Complete Menthol Pain Reliever	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		ORCA Products, LLC	openfda.manufacturer_name
ndc	package	82939-000-01	openfda.package_ndc
ndc	package	82939-000-02	openfda.package_ndc
ndc	product	82939-000	openfda.product_ndc
ndc11	package	82939000002	derived:openfda.package_ndc
ndc11	package	82939000001	derived:openfda.package_ndc
rxcui		2611702	openfda.rxcui
spl id		0c06e3d2-4481-f4b5-e063-6394a90a0608	id
spl set id		99990e27-d66b-4d61-97f2-6a76066eb8b8	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 Do not use this product for more than 7 days unless directed by a dentist or doctor. When using this product do not exceed recommended dosage. Stop use and ask a doctor if sore mouth symptoms do not improve in 7 days irritation, pain, or redness persists or worsens swelling, rash, or fever develops If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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