RICHTOFIT RAPID ACTIVE ARTHRITIS

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 ARTHRITIS
Generic name: MENTHOL AND CAMPHOR
Manufacturer: RICHTOFIT LIMITED LIABILITY COMPANY
Product type: HUMAN OTC DRUG
SPL set ID: 4b1cdab1-3e50-4ec3-e063-6394a90af75e
SPL ID: 4cdb9284-9194-8e5b-e063-6294a90a05fb
Version: 2
Effective date: 2026-03-12
Source export date: 2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:01

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		RICHTOFIT RAPID ACTIVE ARTHRITIS	openfda.brand_name
generic name		MENTHOL AND CAMPHOR	openfda.generic_name
manufacturer name		RICHTOFIT LIMITED LIABILITY COMPANY	openfda.manufacturer_name
ndc	package	87384-058-10	openfda.package_ndc
ndc	product	87384-058	openfda.product_ndc
ndc11	package	87384005810	derived:openfda.package_ndc
rxcui		2739008	openfda.rxcui
spl id		4cdb9284-9194-8e5b-e063-6294a90a05fb	id
spl set id		4b1cdab1-3e50-4ec3-e063-6394a90af75e	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	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, or 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.