24 7 Relief and Recovery Pain Relieving

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: 24 7 Relief and Recovery Pain Relieving
Generic name: MENTHOL, UNSPECIFIED FORM
Manufacturer: Triplicare Inc
Product type: HUMAN OTC DRUG
SPL set ID: 53ca807b-3ec2-4b5e-aa5a-6dcb756bb423
SPL ID: 50acffaf-7b87-df5e-e063-6394a90ad6b5
Version: 1
Effective date: 2026-04-30
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 06:18:54

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		24 7 Relief and Recovery Pain Relieving	openfda.brand_name
generic name		MENTHOL, UNSPECIFIED FORM	openfda.generic_name
manufacturer name		Triplicare Inc	openfda.manufacturer_name
ndc	package	87656-964-04	openfda.package_ndc
ndc	package	87656-964-32	openfda.package_ndc
ndc	product	87656-964	openfda.product_ndc
ndc11	package	87656096432	derived:openfda.package_ndc
ndc11	package	87656096404	derived:openfda.package_ndc
rxcui		1655936	openfda.rxcui
spl id		50acffaf-7b87-df5e-e063-6394a90ad6b5	id
spl set id		53ca807b-3ec2-4b5e-aa5a-6dcb756bb423	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. Use only as directed. Keep away from excessive heat or flame. When using this product: Avoid contact with the eyes or mucous membranes. Do not apply to wounds or damaged skin. Do not use with other ointments, creams, sprays or liniments. Do not apply to irritated skin or if excessive irritation develops. Do not bandage. Do not use with heating pad or device. Wash hands after use with cool water. Stop use and ask doctor if: Condition worsens, or if symptoms persist for more than 7 days, or clear up and return. If pregnant or breast-feeding: Ask a health professional before use. Keep out of the reach of children. If accidentally ingested, get medical help or contact Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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