Menthol, Camphor

Manufacturer
Chemco Corporation
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:29:11

Label at a glance#

ProductMenthol, Camphor
Active ingredientMENTHOL, UNSPECIFIED FORM, CAMPHOR (NATURAL)
Label structure10 sections

Indications and uses

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

Dosage and administration

Adults and children over 12 years of age; apply a thin layer to 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 unless directed by doctor/physician

Storage and handling

Store at room temperature 15° - 30°C (59° - 86°F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%
Camphor 3%

OTC - PURPOSE SECTION

External Analgesic
Pain Relieving

Uses

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Use only as directed. For external use only. Do not bandage tightly. Do not use with heating pad,
pack, wrap, hot water bottle or any heating element. Keep away from children. Package not child
resistant. In case of accidental ingestion, contact doctor immediately. If prone to allergic reaction to
the product, consult to a doctor before using.

OTC - WHEN USING SECTION

Avoid contact with eyes, mucous membranes, rashes, wounds or damaged skin. Do not apply on
nose and genital area. If rash, redness or itchiness results; discontinue use and consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away from children. Package not child
resistant. In case of accidental ingestion, contact doctor immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years of age;

  • apply a thin layer to 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 unless directed by doctor/physician

Other information

STORAGE AND HANDLING SECTION

Store at room temperature 15° - 30°C (59° - 86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Alcohol Denat, Stearic Acid, Paraffinum Liquidum, Cetearyl Alcohol, Polysorbate 60, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Glycereth-26, Tocopheryl Acetate, Caprylic/Capric Triglyceride, Propylene Glycol, Diazolidinyl Urea, Stearyl Alcohol, Polysorbate 20, Triethanolamine, Cannabis Sativa Seed Oil, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Benzotriazolyl Dodecyl p-Cresol, Methylparaben, Propylparaben, FD&C YELLOW No.5 (CI 19140), FD&C Blue No.1 (CI 42090).

PAIN RELIEF CREAM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CREAMCREAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49283-576-02Menthol, Camphor57 g in 1 JARCREAM572

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49283-57649283-576-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
Menthol, CamphorMENTHOL, CAMPHORChemco Corporation472fb097-92e5-c230-e063-6294a90ab33a2025-12-30WarningsExact identifier
ndc (package): 49283-576-02
ndc (product): 49283-576
ndc11 (package): 49283057602
spl id: 472f3d60-3c1a-3152-e063-6294a90a2928
spl set id: 472fb097-92e5-c230-e063-6294a90ab33a

Reported adverse events (FAERS/openFDA)#

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