FDA.reportPublic FDA data

Terrasil Arthritis Cream

Manufacturer
Aidance Skincare & Topical Solutions, LLC | Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions
Effective date
2021-08-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:38:36

Label at a glance#

ProductTerrasil Arthritis Cream
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure8 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with arthritis.

Dosage and administration

Adults and children 12 years of age and older. Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age - consult a physician. May stain fabrics.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with arthritis.

Warnings

WARNINGS SECTION

For external use only.
Do not use on wounds or damaged skin and avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed consult a physician.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older. Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age - consult a physician. May stain fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Chamomile oil, cotton seed oil, emulsifying wax, jojoba oil, magnesium oxide, olive oil, purified water, sage oil, shea butter, silver stearate, sorbic acid (preservative), vitamin B oil, zinc oxide.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-19724909-197-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETYL STEARATE06RI5UQA7LIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
CHAMOMILE FLOWER OIL60F80Z61A9IACT
COTTONSEED OILH3E878020NIACT
JOJOBA OIL724GKU717MIACT
MAGNESIUM OXIDE3A3U0GI71GIACT
OLIVE OIL6UYK2W1W1EIACT
WATER059QF0KO0RIACT
SAGE OILU27K0H1H2OIACT
SHEA BUTTERK49155WL9YIACT
ZINC OXIDESOI2LOH54ZIACT
SORBIC ACIDX045WJ989BIACT
SILVER OXIDE897WUN6G6TIACT
PANTHENOLWV9CM0O67ZIACT

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
193cdcaf-88e6-201d-e063-6394a90a55bd78a16831-f0c3-4fae-9b4a-2bce3fe73d2f2024-05-24WarningsExact identifier
spl set id: 78a16831-f0c3-4fae-9b4a-2bce3fe73d2f

Reported adverse events (FAERS/openFDA)#

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