MENTHOL, CAMPHOR

Manufacturer
SUNSET NOVELTIES, INC
Effective date
2025-11-21
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:17:37

Label at a glance#

ProductMENTHOL, CAMPHOR
Active ingredientMENTHOL, 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

For external use only.
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.

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.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away from children. Package not child resistant.

OTHER INFORMATION:

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

Aqua, Paraffinum Liquidum, Alcohol Denat, Stearic Acid, Cetearyl Alcohol, Polysorbate 60, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Glycereth-26, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Tocopheryl Acetate, Cannabis Sativa Seed Oil, Stearyl Alcohol, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Polysorbate 20, Triethanolamine, 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 #1 Powder (CI 42090), Linalool, Limonene, Benzyl Benzoate, Coumarin, Geraniol.

GREEN FARM PAIN RELIEF CREAM 8 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GREEN FARM PAIN RELIEF CREAM 8GREEN FARM PAIN RELIEF CREAM 8

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72937-103-082022-07-12C16284748780-1d6a99b39-e318-a426-e053-dadaa90af4c272937-103-08

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72937-103-08MENTHOL, CAMPHOR226 g in 1 BOTTLECREAM2266

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72937-10372937-103-08

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
MENTHOL, CAMPHORMENTHOL, CAMPHORSUNSET NOVELTIES, INCb0edd9d9-951f-d3dd-e053-2995a90a8d5a2025-11-21WarningsExact identifier
ndc (package): 72937-103-08
ndc (product): 72937-103
ndc11 (package): 72937010308
spl id: 44250376-aa87-fcb7-e063-6394a90a21c1
spl set id: b0edd9d9-951f-d3dd-e053-2995a90a8d5a

Reported adverse events (FAERS/openFDA)#

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