CANNABICIN Joint & Muscle Pain Relief Cream

Manufacturer
CN Brands, LLC
Effective date
2018-03-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:00:44

Label at a glance#

ProductCANNABICIN Joint and Muscle Pain Relief
Active ingredientMENTHOL
Label structure7 sections

Dosage and administration

• Adults and children 12 years of age or older: Apply to affected area not more than three to four times daily. • Massage into affected area until fully absorbed. • Children under 12 years of age: consult a physician.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 4.00%

OTC - PURPOSE SECTION

Topical Analgesic

Indications:

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with:

• arthritis • simple backache • sprains • bruises  • strains

Warnings:

WARNINGS SECTION

• For external use only.

• Avoid contact with eyes or mucous membranes.

• If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• If swallowed, contact physician or Poison Control center.

• Do not apply to wounds a damaged skin.

• Do not bandage tightly or use with a heating pad.

Do not use

OTC - DO NOT USE SECTION

if pregnant or breast feeding, contact physician prior to use.

Directions:

DOSAGE & ADMINISTRATION SECTION

• Adults and children 12 years of age or older: Apply to affected area not more than three to four times daily.

• Massage into affected area until fully absorbed.

• Children under 12 years of age: consult a physician.

Additional Information:

SPL UNCLASSIFIED SECTION

• Store at room temperature, in a cool, dry place.
• Do not use if tamper evident seal has been broken.

Other Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Concentrate (Leaf), Eugenia Caryophyllus (Clove Bud) Oil, Piper Nigrum (Unripe Black Papper Seed) Oil, Glyceryl Stearate, Methylsulfonylmethane (MSM), Glycerin (vegetabl origin), Stearyl Alcohol, Palmitic Acid Monoethanolamide, Cannabis Sativa (Hemp Stalk/Seed) Oil, Polysorbate-20, Propylene Glycol, Sorbitan Stearate, Stearic Acid, Helianthus Annuus (Sunflower seed) Oil, Cetyl Alcohol, Ethoxydiglycol, Arnica Montana Flower Extract, Curcuma longa (Turmeric) Extract, Cinnamomum Cassia Bark Oil, Boswellia Serrata (Gum) Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Magnesium Sulfate, Mentha Piperita (Peppermint) Oil, Carbomer, Phenoxyethanol, Ethylhexylglycerin, Sodium Hydroxide.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72181-17872181-178-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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
dc2480d4-700f-7054-e053-2a95a90a97b5eb7d8270-1596-411a-bfaf-bb03b7ca6f702022-04-08WarningsExact identifier
spl set id: eb7d8270-1596-411a-bfaf-bb03b7ca6f70

Reported adverse events (FAERS/openFDA)#

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