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Brand-name over-the-counter medicine

Satohap

Generic names: Camphor (synthetic), levomenthol and methyl salicylate · Camphor (synthetic), capsaicin and levomenthol

Company: Sato Pharmaceutical Co., Ltd.

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Read the label on your package, and ask a pharmacist if you are not sure a medicine is right for you or your child.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Satohap?
Satohap is a brand name of Camphor (synthetic), levomenthol and methyl salicylate and Camphor (synthetic), capsaicin and levomenthol, an over-the-counter medicine. The FDA NDC Directory lists 6 Satohap products in 5 strengths and forms.
Who makes Satohap?
Sato Pharmaceutical Co., Ltd. lists 5 of the 6 Satohap products in the FDA NDC Directory.
Is there a generic or store brand of Satohap?
Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Satohap product, 1 of them generic or store brands. Ask your pharmacist whether one is right for you.
Has Satohap been recalled?
No recall linked to Satohap products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Satohap is

Each Satohap 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.

Camphor (synthetic), levomenthol and methyl salicylate · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
camphor (synthetic) 5 mg · levomenthol 4 mg · methyl salicylate 8 mg
patch (topical)
Satohap 1 product, 1 company DailyMed
camphor (synthetic) 5% · levomenthol 4% · methyl salicylate 10%
lotion (topical)
Satohap None listed DailyMed
camphor (synthetic) 5% · levomenthol 4% · methyl salicylate 10%
spray (topical)
Satohap None listed DailyMed
camphor (synthetic) 5% · levomenthol 6% · methyl salicylate 10%
lotion (topical)
Satohap Cool Type None listed DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Camphor (synthetic), levomenthol and methyl salicylate →

Camphor (synthetic), capsaicin and levomenthol · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
camphor (synthetic) 3.1% · capsaicin 0.025% · levomenthol 6%
patch (topical)
Satohap Cool and Hot Pads, SATOHAP COOL and HOT None listed DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Camphor (synthetic), capsaicin and levomenthol →

FDA approval

Satohap 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 Satohap

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Satohap products.

  • Sato Pharmaceutical Co., Ltd.5 products
  • Sato Pharmaceuticals Co., Ltd.1 product

Recalls

No recall linked to Satohap products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. 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.

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