FORS PAIN RELIEF CREAM

Manufacturer
FORS LLC
Effective date
2022-01-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:16:54

Label at a glance#

ProductFORS PAIN RELIEF
Active ingredientMENTHOL, CAPSAICIN
Label structure8 sections

Indications and uses

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

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area not ore than 3 to 4 times daily. Children under 2 years of age: consult doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 4.00%

Capsaicin 0.035%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

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

Warnings:

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. Rinse with water to remove. 
  • Do not bandage tightly.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash or irritation develops and lasts. 
  • Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: Apply to affected area not ore than 3 to 4 times daily.
  • Children under 2 years of age: consult doctor.

Other information:

SPL UNCLASSIFIED SECTION

Store at 20-25 C (68-77 F) and protect from moisture.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alky Acrylate Crosspolymer, Allantoin, Aloe Barbadensis Leaf(Aloe Vera Gel) Juice, Aqua (Deionized Water), Amica Montana Flower Extract, Boswellia Serrata Extract, Butylene Glycol, *Cannabidiol (CBD), Caprylic/Capric Triglyceride, Celeareth-20, Cetyl Alcohol, Ethylhexyglycerin, Eucalyptus Globulus Oil, Glycerin, Clyceryl Stearate,Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurale Copolymer, Ilex
Paraguayensis (Yerba Mate) Extract, Methylsulfonylmethane (MSM), Mineral Oil, Phenoxyethanol, Polysorbate-20, Polysorbate-60, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Squalane Stearic Acid, Triethanolamine, Tocopheryl Acetate (Vitamin E).

Questions?

OTC - QUESTIONS SECTION

1-800-210-7924

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81765-18481765-184-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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
d597f26b-a675-5fb1-e053-2995a90a4f2ff4959721-dc6b-4f83-80ec-4f285eaa48352022-01-14WarningsExact identifier
spl id: d597f26b-a675-5fb1-e053-2995a90a4f2f
spl set id: f4959721-dc6b-4f83-80ec-4f285eaa4835

Reported adverse events (FAERS/openFDA)#

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