Arthritis Relief

Manufacturer
Geiss, Destin & Dunn, Inc
Effective date
2024-01-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:14:02

Label at a glance#

ProductArthritis Relief Maximum Strength
Active ingredientTROLAMINE SALICYLATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Trolamine Salicylate 10%

OTC - PURPOSE SECTION

Topical Analgesic.

DOSAGE & ADMINISTRATION SECTION

Temporarily relieves minor pain associated with arthritis, simple backache, muscle strains, sprains, and cramps.

WARNINGS SECTION

For external use only.

Allergy Alert: if prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

When using this product use only as directed, avoid taking a bath or shower within 1 hour before or after applying, do not bandage or use with a heating pad, avoid contact with eyes or mucous membranes, do not apply to wounds or damaged skin.

Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days, if symptoms clear up and occur again within a few days, or if irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health care professional before use.

INDICATIONS & USAGE SECTION

Adults and children 12 years of age: apply generously to the affected area, massage into painful area until thoroughly absorbed into the skin, repeat as necessary, but not more than 3 to 4 times daily. Children under 12 years of age: ask a doctor.

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Cetyl Alcohol, Glycerin, Methylparaben, Mineral Oil, Potassium Phosphate, Propylparaben, Stearic Acid, Triethanolamine, Water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50804-214-032024-01-17C16284748780-1f386c649-9e75-0266-e053-dadaa90a7c1aArthritis Relief, 10% Trolamine Salicylate
50804-214-032023-01-30C16284748780-1f386c649-9e75-0266-e053-dadaa90a7c1aArthritis Relief, 10% Trolamine Salicylate

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50804-214ARTHRITIS RELIEF MAXIMUM STRENGTH (TROLAMIN SALICYLATE 10%) CREAM [GEISS, DESTIN & DUNN, INC]2Legacy NDC20240118_aca0a812-b119-0a0e-e053-2995a90adb4b.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50804-21450804-214-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
3f1a55fb-da50-ff4b-e063-6294a90aae2caca0a812-b119-0a0e-e053-2995a90adb4b2025-09-18WarningsExact identifier
spl set id: aca0a812-b119-0a0e-e053-2995a90adb4b

Reported adverse events (FAERS/openFDA)#

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