Liberdol Topical Analgesic Spray
FDA Label NDC 71262-008

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Viaderma Distribution, Inc for the product Liberdol Topical Analgesic (NDC 71262-008). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, ask a doctor before use if you have:, when using this product:, stop use and ask a doctor if:, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Methyl Salicylate 300mg

Menthol 100mg

Camphor 40mg

Purpose

Analgesic

Uses

Soothing on-the-go tempoary relief from minor aches and pains of sore muscles and joint associated with:

  • arthritis
  • backache
  • strains
  • sprains

Warnings

For external use only. Flammable: Keep away form excessive heat or open flame

Ask A Doctor Before Use If You Have:

Sensitive skin, are pregnant or are bleeding

When Using This Product:

  • Avoid contact with eyes or mucus membranes
  • Do not apply to open wounds or damaged skin
  • Do not use with other ointments, creams, sprays or liniments
  • Do not apply to irritated skin, or if excessive irritation develops
  • Do not bandage
  • Do not use with heating pad or device

Stop Use And Ask A Doctor If:

Condition worsens or if symptoms persist more than 7 days, or clear up or reoccur

Keep Out Of Reach Of Children.

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

Directions

  • Adults and children 2 years of age an older: Apply to affected areas not more than 4 times daily
  • Children under 2 years of age: Consult a physician

Other Information

  • Store in a cool dry place out of direct sunlight

Inactive Ingredients

acetic acid, arnica montana flower extract, ascorbic acid, chlorhexidine gluconate, cholecalciferol, dimethyl sulfoxide, dipropylene glycol, glucono delta lactone, glycerin, histidine, hydroxethyl cellulose, magnesium stearate, sodium hydroxide, sorbic acid, stearic acid, water

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