HEATING PAIN RELIEF

Manufacturer
CHEMCO CORPORATION
Effective date
2026-02-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:36:47

Label at a glance#

ProductHEATING PAIN RELIEF
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure12 sections

Dosage and administration

Adults and Children over 12 years Apply a small amount on the affected area. Massage in circular motion, let set for a few seconds.. Repeat as necessary, but no more than 3 to 4 times daily. Wash hands with soap and water after use. Children under 12 years of age consult a doctor.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate 18%

Menthol 10%

OTC - PURPOSE SECTION

Topical Analgesic.

Use

INDICATIONS & USAGE SECTION

Aid for temporary local relief of minor pain in muscles or joints.

WARNINGS SECTION

For external use only. · Ask a doctor before use if you have redness over affected area

OTC - WHEN USING SECTION

Use only as directed
Do not bandage tightly or use with a heating pad
Avoid contact with eyes and mucous membranes
Do not apply to wounds or damaged, broken or irritated skin
If you experience an allergic reaction, discontinue use and consult a doctor.

Do not expose the area treated with product to heat or direct sunlight.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Condition worsens
Redness is present
Irritation develops
Symptoms persist for more than 7 days or clear up occur again within a few days

You experience signs injury, such as pain, swelling or blistering where the product was applied.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years

Apply a small amount on the affected area.
Massage in circular motion, let set for a few seconds..
Repeat as necessary, but no more than 3 to 4 times daily.
Wash hands with soap and water after use.

Children under 12 years of age consult a doctor.

Other information

OTHER SAFETY INFORMATION

Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

INACTIVE INGREDIENT SECTION

Water (Aqua), Paraffinum Liquidum, Cetyl Alcohol, Glyceryl Stearate, Stearic Acid, Glycereth-26, Dimethicone, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Caprylyl Glycol, Hexylene Glycol, Stearyl Alcohol, Triethanolamine, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Cannabis Sativa (Hemp) Seed Oil, Phenoxyethanol, FD&C Yellow No.6 (CI 15985).

GENERIC LABEL - ULTRA STRENGHT PAIN RELIEF CREAM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HEATING PAIN RELIEF CREAMHEATING PAIN RELIEF CREAM

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49283-579-20HEATING PAIN RELIEF59 mL in 1 TUBECREAM593

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49283-57949283-579-20

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
HEATING PAIN RELIEFMETHYL SALICYLATE, MENTHOLCHEMCO CORPORATION4a05f02e-e882-2cb2-e063-6394a90ad3282026-02-04WarningsExact identifier
ndc (package): 49283-579-20
ndc (product): 49283-579
ndc11 (package): 49283057920
spl id: 4a05f4ed-dd2e-601d-e063-6294a90a1d12
spl set id: 4a05f02e-e882-2cb2-e063-6394a90ad328

Reported adverse events (FAERS/openFDA)#

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