RICHTOFIT RAPID ACTIVE ARTHRITIS

Manufacturer
RICHTOFIT LIMITED LIABILITY COMPANY
Effective date
2026-03-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:50:27

Label at a glance#

ProductRICHTOFIT RAPID ACTIVE ARTHRITIS
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure6 sections

Label contents#

Full prescribing information#

Drug Facts

INSTRUCTIONS FOR USE SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 5% – External Analgesic

Camphor 4% – External Analgesic

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Use only as directed.
Avoid contact with eyes or mucous membranes.

Do not use

OTC - DO NOT USE SECTION

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

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If accidentally ingested, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: apply to affected area not more than 4 times daily.
Children under 2 years of age: ask a doctor.

Other information

OTHER SAFETY INFORMATION

Store in a cool, dry place.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cetearyl Alcohol, Anthemis Nobilis Flower Oil, Chamomilla Recutita Flower Extract, Chamomilla Recutita Flower Oil, Humulus Lupulus Extract, Juglans Regia Leaf Extract, Lavandula Angustifolia Flower/Leaf/Stem Extract, Potentilla Anserina Extract, Quercus Robur Bark Extract, Salix Alba Bark Extract, Salvia Officinalis Leaf Extract, Glycerin, Cocos Nucifera Oil, Polysorbate 20, Phenoxyethanol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tocopherol, Sodium Hydroxide, Ethylhexylglycerin.

Questions or Comments

OTC - QUESTIONS SECTION

Call 1-832-709-0788 Monday through Friday 9 AM to 5 PM CST or visit www.richtofit.us.

use

INDICATIONS & USAGE SECTION

Temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains, and bruises.

Purpose

OTC - PURPOSE SECTION

External Analgesic

PRINCIPAL DISPLAY PANEL CONTENTS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RICHTOFIT RAPIDACTIVE ARTHRITIS GEL

NDC 87384-058-10
Cooling Pain Relief
Intensive Formula
RapidActive Arthritis Gel
Soothing and Revitalizing
Non Greasy – Fast Acting

Net Wt. 3 oz (85 g)

Richtofit Complex Formula

Herbal Extracts
Made in U.S.A.

Descriptive Text

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RICHTOFIT RAPIDACTIVE ARTHRITIS GEL combines the fast-acting cooling power of Menthol and Camphor with the restorative effects of the Richtofit Herbal Complex, a European blend trusted for over 40 years. This smooth, non-greasy gel helps soothe the body by relieving minor muscle and joint aches, easing stiffness, and delivering a cooling sensation that refreshes tired, stressed areas.

Herbal extracts including Chamomile, Lavender, Sage Leaf, Willow Bark, and Walnut Leaf help comfort the skin, soften rough areas, and support a naturally revitalized feel. Ideal for daily use, before or after activity, or anytime the body needs cooling comfort.

Temporary cooling relief of minor aches and pains.
Soothes the body, easing tension and stressed areas.
Revitalizing herbal effects refresh tired muscles and joints, reducing stiffness.
Herbal extracts help comfort and condition the skin.
Provides both targeted pain relief and body comfort.

Manufacture

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Manufactured in U.S.A. for:
Richtofit Limited Liability Company
611 Choctaw Lane, Suite G
Katy, TX 77494

NDC 87384-058-10
Net Wt. 3 oz (85 g)

TUBE IMAGE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RICHTOFIT RAPID ACTIVE ARTHRITIS GEL TUBERICHTOFIT RAPID ACTIVE ARTHRITIS GEL TUBE

BOX IMAGE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RICHTOFIT RAPID ACTIVE ARTHRITIS GEL BOXRICHTOFIT RAPID ACTIVE ARTHRITIS GEL BOX

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2739008camphor 4 % / menthol 5 % Topical GelPSN2
2739008camphor 0.04 MG/MG / menthol 0.05 MG/MG Topical GelSCD2
2739008camphor 4 % / menthol 5 % Topical GelSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860015386786GTIN-13: 0860015386786
EAN-13: 0860015386786
GTIN-12: 860015386786
UPC-A: 860015386786
GTIN storage (14 digits): 00860015386786
Richtofit Rapid Active Arthritis Gel tube.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87384-058-10RICHTOFIT RAPID ACTIVE ARTHRITIS85 g in 1 TUBEGEL852
87384-058-10RICHTOFIT RAPID ACTIVE ARTHRITIS1 in 1 CARTONGEL12

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87384-05887384-058-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RICHTOFIT RAPID ACTIVE ARTHRITISMENTHOL AND CAMPHORRICHTOFIT LIMITED LIABILITY COMPANY4b1cdab1-3e50-4ec3-e063-6394a90af75e2026-03-12WarningsExact identifier
ndc (package): 87384-058-10
ndc (product): 87384-058
ndc11 (package): 87384005810
spl id: 4cdb9284-9194-8e5b-e063-6294a90a05fb
spl set id: 4b1cdab1-3e50-4ec3-e063-6394a90af75e

Reported adverse events (FAERS/openFDA)#

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