ReLeaf Arthritis Balm

Manufacturer
Skidmore Companies
Effective date
2023-06-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:29:18

Label at a glance#

ProductReLeaf Arthritis Balm Extra Strength
Active ingredientMETHYL SALICYLATE
Label structure10 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Label contents#

Full prescribing information#

Active IIngredients

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate (oil of wintergreen) - 2%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with:

simple backache
arthritis
strains
bruises
sprains

Warnings

WARNINGS SECTION

Ask A Doctor/Pharmacist:

OTC - ASK DOCTOR/PHARMACIST SECTION

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes

When Using

OTC - WHEN USING SECTION

When using this product: Avoid Contact with eyes, acoid use on deep wounds, avoid if your allergic to listed ingredients

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health care professional before use

Directins

DOSAGE & ADMINISTRATION SECTION

Dosage: Apply to affected area 1-4 times daily. (Or as needed)

Stop Use

OTC - STOP USE SECTION

Stop Use and Consult a Doctor uf: Condition worsens, symptoms last more than 7 days, condition clears up but occurs again in a few days, rash or irritation occurs.

Other Information

OTHER SAFETY INFORMATION

Store at 66-92 Degrees Farenheit. Avoid direct sunlight.

INACTIVE INGREDIENT SECTION

Shea Butter, Grapeseed Oil, Vitamin E Oil, Cannabidiol, Beeswax

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Releaf Salve LOGOReleaf Salve LOGO

Products#

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DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83517-00183517-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
069afc12-0eea-5b8a-e063-6394a90a7699fdb53658-7fb9-dbe6-e053-6294a90a39392023-09-30WarningsExact identifier
spl set id: fdb53658-7fb9-dbe6-e053-6294a90a3939

Reported adverse events (FAERS/openFDA)#

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