Quick answers
- What is Eagle?
- Eagle is a brand name of Menthol and methyl salicylate, Camphor (synthetic) and menthol and Camphor (synthetic), menthol and methyl salicylate, an over-the-counter medicine. The FDA NDC Directory lists 33 Eagle products in 11 strengths and forms.
- Who makes Eagle?
- Borden Company (Private) Limited lists 17 of the 33 Eagle products in the FDA NDC Directory.
- Is there a generic or store brand of Eagle?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Eagle product, 1 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Eagle been recalled?
- No recall linked to Eagle products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Eagle is
Each Eagle product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Menthol and methyl salicylate · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| menthol 13.5% · methyl salicylate 29.95% ointment (topical) | Eagle Brand Muscular Balm | 1 product, 1 company | DailyMed |
| menthol 133.4 mg/mL · methyl salicylate 276 mg/mL liniment (topical) | Eagle Brand Muscle Rub | None listed | — |
| menthol 14% · methyl salicylate 15% oil (topical) | Eagle Medicated Oil Refreshing | None listed | DailyMed |
| menthol 14.5% · methyl salicylate 30% liquid (topical) | Eagle Brand Muscle Rub, Eagle Extra Strength | None listed | DailyMed |
| menthol 14.5% · methyl salicylate 30% oil (topical) | Eagle Medicated, Eagle Brand Medicated Roll On, Eagle Brand Medicated Oil | None listed | DailyMed |
| menthol 5% · methyl salicylate 1% patch (topical) | Eagle Brand Medicated Plaster | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Menthol and methyl salicylate →
Camphor (synthetic) and menthol · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| camphor (synthetic) 11% · menthol 15% ointment (topical) | Eagle Green Balm, Eagle Balm | None listed | DailyMed |
| camphor (synthetic) 2.2% · menthol 14% oil (topical) | Eagle Brand Medicated Oil Refresh, Eagle Brand Medicated Roll On Refresh | None listed | DailyMed |
| camphor (synthetic) 4% · menthol 15.5% ointment (topical) | Eagle Brand Eagle Balm | None listed | — |
Its page quotes the Drug Facts label and lists every brand and store brand: Camphor (synthetic) and menthol →
Camphor (synthetic), menthol and methyl salicylate · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| camphor (synthetic) 6.846% · menthol 15.648% · methyl salicylate 34.23% oil (topical) | Eagle Brand Medicated Oil Aromatic | None listed | DailyMed |
| camphor (synthetic) 7% · menthol 16% · methyl salicylate 35% oil (topical) | Eagle Brand Medicated Oil Aromatic, Eagle Medicated Aromatic, Eagle Brand Medicated Roll On Aromatic | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Camphor (synthetic), menthol and methyl salicylate →
FDA approval
Eagle products are sold under an FDA over-the-counter monograph: rules that set the allowed active ingredients, strengths and label wording, so these products do not need an individual FDA approval.
Companies that list Eagle
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Eagle products.
- Borden Company (Private) Limited17 products
- PT. Eagle Indo Pharma11 products
- Eagle Indo Pharma, PT4 products
- Eagle Indo Pharma1 product
Recalls
No recall linked to Eagle products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.