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Menthol, Camphor drug information

MENTHOL, CAMPHOR
SUNSET PAIN RELIEF · TOPICAL

Product NDC: 72937-013

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameMENTHOL, CAMPHOR
Labeler / manufacturerSUNSET PAIN RELIEF
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC72937-013
Label effective date2026-08-20

Official product label reference

Menthol, Camphor — SUNSET PAIN RELIEF

This page contains 11 source sections for MENTHOL, CAMPHOR, topical route. Label set 5980c527-6bcb-a846-e063-6294a90a0788, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

USE For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, sprains and strains.

Purpose

​Topical Analgesic
Dosage and administration — label text
Directions Adults and Children over 12 years Apply a thin layer to the affected area and rub gently not more than 3 to 4 times a day. Wash hands with soap and water after use. Children under 12 years of age: do not use, consult a doctor.
Warnings
For external use only. · Ask a doctor before use if you have redness over affected area
Active ingredient
Camphor 3% Menthol 10%
While using this medicine
Use only as directed. Do not bandage tightly. Do not use with heating pad, pack, wrap, hot water bottle or any heating element. In case of accidental ingestion, contact doctor immediately. If prone to allergic reaction to the product, consult to a doctor before using.
When to stop use and seek help
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.
Pregnancy or breast feeding
If pregnant or breast – feeding Ask a health professional before use.
Child safety
If swallowed, get medical help, or contact a Poison Control Center right away.
Other safety information
Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).
Inactive ingredient
Water (Aqua), Paraffinum Liquidum, Alcohol Denat, Stearic Acid, Cetearyl Alcohol, Polysorbate 60, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Glycereth-26, Tocopheryl Acetate, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Cannabis Sativa Seed Oil, Stearyl Alcohol, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Polysorbate 20, Triethanolamine, Fragrance (Parfum), Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Sodium Benzotriazolyl Butylphenol Sulfonate, Buteth-3, Tributyl Citrate, Cannabidiol, FD&C Blue No.1 (CI 42090), Linalool, Limonene, Benzyl Benzoate, Coumarin, Geraniol.

Official sources and product identifiers

Substances listed: MENTHOL, UNSPECIFIED FORM, CAMPHOR (NATURAL)

Package NDC codes

72937-013-08

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.