MENTHOL, CAMPHOR

Manufacturer
SUNSET NOVELTIES, INC
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:45:22

Label at a glance#

ProductMENTHOL, CAMPHOR
Active ingredientMENTHOL, CAMPHOR, (-)-
Label structure11 sections

Indications and uses

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

Dosage and administration

Adults and Children over 12 years: Apply a small amount on the area to be. Massaged in a circular motion until absorbed. Repeat as needed, but no more than 3 to 4 times per day. Store tightly closed in a dry place at room temperature between 59°-86° F (15°-30° C). Wash hands with soap and water after use.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 6%

Camphor 2%

OTC - PURPOSE SECTION

Topical Analgesic

Pain Relieving

USES:

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

WHEN USING THIS PRODUCT:

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
A transient burning sensation or redness may occur upon application but generally disappears in several days
If you experience an allergic reaction, discontinue use, and consult a physician
Do not expose the area treated with product to heat or direct sunlight.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

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.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years:

Apply a small amount on the area to be.
Massaged in a circular motion until absorbed.
Repeat as needed, but no more than 3 to 4 times per day.
Store tightly closed in a dry place at room temperature between 59°-86° F (15°-30° C).

Wash hands with soap and water after use.

INACTIVE INGREDIENT SECTION

Aqua, Alcohol Denat, Propylene Glycol, Salicylic Acid, Glycerin, Polysorbate 20, Carbomer, Sodium Hydroxide, Mentha Arvensis Herb Oil, Rosmarinus Officinalis (Rosemary) Oil, Thymus Vulgaris (Thyme) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Cannabis Sativa Seed Oil, Benzyl Alcohol, Sorbic Acid, Cannabidiol, FD&C Blue. 1 Powder (CI 42090), FD&C Yellow. 5 (CI 19140).

GREEN FARM COOLING RELIEF GEL 1.7oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GREEN FARM COOLING RELIEF GEL 1.7GREEN FARM COOLING RELIEF GEL 1.7

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72937-600-172025-11-24C16284748780-1d6a99b39-4820-a426-e053-dadaa90af4c272937-600-17
72937-600-172025-01-30C16284748780-1d6a99b39-4820-a426-e053-dadaa90af4c272937-600-17
72937-600-172022-12-07C16284748780-1d6a99b39-4820-a426-e053-dadaa90af4c272937-600-17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72937-600MENTHOL, CAMPHOR GEL [SUNSET NOVELTIES, INC]4Legacy NDC20221208_afec7d2c-ee59-34ea-e053-2a95a90a3977.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72937-60072937-600-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
44618dba-dd29-6982-e063-6294a90aef19afec7d2c-ee59-34ea-e053-2a95a90a39772025-11-24WarningsExact identifier
spl set id: afec7d2c-ee59-34ea-e053-2a95a90a3977

Reported adverse events (FAERS/openFDA)#

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