Active Ingredients
- Menthol 14.5%
- Methyl Salicylate 30%
Eagle Brand Oil
FDA Label NDC 60954-020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pt. Eagle Indo Pharma for the product Eagle Brand (NDC 60954-020). 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, do not use, ask a doctor before use if, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical analgesic
Uses
Temporarily relieves the minor aches and pains of muscles and joints associated with:
- simple backache
- strains
- bruises
- sprains
Warnings
For external use only
Do Not Use
- on wounds or damage skin
- with a heating pad
Ask A Doctor Before Use If
you have redness over affected area
When Using This Product
- avoid contact with eyes or mucous membranes
- do not bandage tightly
Stop Use And Ask A Doctor If
- condition worsens or symptoms persist for more than 7 days
- symptoms clear up and occur again within a few days
- excessive skin irritation occurs
Keep Out Of Reach Of Children
Avoid accidental poisoning.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Use only as directed
- adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
- children under 2 years of age: ask a doctor
Inactive Ingredients
Chlorophyll, ethyl alcohol, mineral oil, rose oil
Questions?
1-800-777-6717 or 1-800-645-0769
Package Label
8ml NDC: 60954-020-08
* Please review the disclaimer below.
