Active Ingredient
Menthol 14.5%
Methyl Salicylate 30.0%
Eagle Oil
FDA Label NDC 43405-006
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 43405-006). 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, 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
Purpose
Topical Analgesic
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
■ excessive skin irritation develops
■ pain worsens or does not approve within 7 days, or clears up and apperas again in a few days
Keep This Drug Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
■ Adults and children 2 years and over: apply to affected area not more than 3 to 4 time daily.
■ Children under 2 years of age: ask a doctor
Inactive Ingredients
D&C Yellow No. 11, D&C Green No. 6, ethyl alcohol, mineral oil, rose oil
* Please review the disclaimer below.
