Active Ingredients
Menthol 14%
Methyl Salicylate 15%
Eagle Medicated Oil
FDA Label NDC 43405-102
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 Medicated Oil (NDC 43405-102). 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 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
External Analgesic
External Analgesic
Uses
For the temporary relief of minor pains and aches of muscles and joints associated with ■simple backache ■arthritis ■strains ■bruises ■ sprains
Warnings
For external use only
When Using This Product
■ avoid getting into the eyes or on mucous membranes
■ do not apply to wounds and damaged skin
■ do not bandage tightly or use with a heating pad
■ do not use otherwise tha as directed
Stop Use And Ask A Doctor If
■ condition worsens, ■ symptoms persist for more than 7 days or clear up and occur again within a few days ■ redness is present
Keep Out Of Reach Of Children
Keep out of reach of children to avoid accidental poisoning. In case of accidental ingestion contact a doctor or Poison Control Center immediately
Directions
■ adults and children 12 years of age: apply to affected area not more than 3 to 4 times daily. ■ children under 12 years of age, consult a doctor before using
Inactive Ingredients
clove oil, eucalyptus oil, fragrance, light mineral oil
* Please review the disclaimer below.
