Eagle Oil
FDA Label NDC 43405-008

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Borden Company (private) Limited for the product Eagle (NDC 43405-008). 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 ingredients, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep this drug out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Menthol 14.5%
Methyl Salicylate 30%


Purpose

Topical Analgesic

Uses

temporarily relieves minor muscle and joint pain due to :

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

For external use only

When Using This Product

  • use only as directed
  • do not get into eyes or mucous membranes
  • do not apply to wound or damaged skin.
  • do not bandage tightly

Stop Use And Ask A Doctor If

  • pain persists for more than 10 days
  • redness is present
  • conditions affect children under 12 years of age
  • discontinue use if excessive irritation of the skin develops

Keep This Drug Out Of Reach Of Children

Do not use otherwise than as directed keep out of the reach of children to avoid accidental poisoning. If swallowed, get medical help or contact a poison control center right away.

Directions

  • Apply to affected area not more than 3 to 4 time daily.
  • This product should not be directed for use by children under 12 years of age.

Inactive Ingredients

Chlorophyll, ethyl alcohol, mineral oil, rose oil

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