RICHTOFIT RAPID ACTIVE LEG AND FOOT

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: RICHTOFIT RAPID ACTIVE LEG AND FOOT
Generic name: MENTHOL
Manufacturer: RICHTOFIT LIMITED LIABILITY COMPANY
Product type: HUMAN OTC DRUG
SPL set ID: 4c357696-ca96-e6ad-e063-6294a90aaadb
SPL ID: 4d2c230a-3bdf-151c-e063-6294a90ade68
Version: 2
Effective date: 2026-03-16
Source export date: 2026-10-27
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:59:14

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		RICHTOFIT RAPID ACTIVE LEG AND FOOT	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		RICHTOFIT LIMITED LIABILITY COMPANY	openfda.manufacturer_name
ndc	package	87384-059-10	openfda.package_ndc
ndc	product	87384-059	openfda.product_ndc
ndc11	package	87384005910	derived:openfda.package_ndc
rxcui		1045482	openfda.rxcui
spl id		4d2c230a-3bdf-151c-e063-6294a90ade68	id
spl set id		4c357696-ca96-e6ad-e063-6294a90aaadb	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: Use only as directed Avoid contact with eyes or mucous membranes. Do not use on wounds, damaged, or irritated skin. Do not bandage or use with a heating pad. Do not use if you are allergic to any of the ingredients. Do not use with other ointments, creams, or sprays. Stop use and ask a doctor if: condition worsens, symptoms persist for more than 7 days, or clear up and occur again within a few days, irritation or redness develops. If pregnant or breast-feeding: ask a health professional before use. Keep out of reach of children: If accidentally ingested, 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.