Quick answers
- What is Stona?
- Stona is a brand name of Acetaminophen, chlorpheniramine, dextromethorphan and phenylephrine, Dextromethorphan, Acetaminophen, chlorpheniramine and dextromethorphan, Dextromethorphan and guaifenesin and Dextromethorphan, guaifenesin and phenylephrine, an over-the-counter medicine. The FDA NDC Directory lists 6 Stona products in 6 strengths and forms.
- Who makes Stona?
- Sato Pharmaceutical Co., Ltd. lists 6 of the 6 Stona products in the FDA NDC Directory.
- Is there a generic or store brand of Stona?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Stona product, 1 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Stona been recalled?
- No recall linked to Stona products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Stona is
Each Stona 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.
Acetaminophen, chlorpheniramine, dextromethorphan and phenylephrine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| acetaminophen 162.5 mg · chlorpheniramine maleate 2 mg · dextromethorphan hydrobromide 10 mg · phenylephrine hydrochloride 5 mg capsule (oral) | Stona-S | None listed | DailyMed |
| acetaminophen 162.5 mg · chlorpheniramine maleate 2 mg · dextromethorphan hydrobromide 10 mg · phenylephrine hydrochloride 5 mg tablet (oral) | Stona | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Acetaminophen, chlorpheniramine, dextromethorphan and phenylephrine →
Dextromethorphan · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dextromethorphan hydrobromide 10 mg lozenge (oral) | Stona | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan →
Acetaminophen, chlorpheniramine and dextromethorphan · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| acetaminophen 325 mg/15 mL · chlorpheniramine maleate 2 mg/15 mL · dextromethorphan hydrobromide 10 mg/15 mL syrup (oral) | Stona for Children | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Acetaminophen, chlorpheniramine and dextromethorphan →
Dextromethorphan and guaifenesin · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dextromethorphan hydrobromide 30 mg/10 mL · guaifenesin 200 mg/10 mL syrup (oral) | Stona Cough | 1 product, 1 company | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan and guaifenesin →
Dextromethorphan, guaifenesin and phenylephrine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dextromethorphan hydrobromide 15 mg · guaifenesin 100 mg · phenylephrine hydrochloride 5 mg tablet (oral) | Stona Cough | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan, guaifenesin and phenylephrine →
FDA approval
Stona 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 Stona
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Stona products.
- Sato Pharmaceutical Co., Ltd.6 products
Recalls
No recall linked to Stona 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.