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Brand-name over-the-counter medicine

Hempvana

Generic names: Trolamine salicylate · Menthol · Lidocaine

Company: Telebrands Corp

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 Hempvana?
Hempvana is a brand name of Trolamine salicylate, Menthol and Lidocaine, an over-the-counter medicine. The FDA NDC Directory lists 5 Hempvana products in 4 strengths and forms.
Who makes Hempvana?
Telebrands Corp lists 5 of the 5 Hempvana products in the FDA NDC Directory.
Is there a generic or store brand of Hempvana?
Yes. The FDA NDC Directory lists 24 other products with the same active ingredients, strength and form as a Hempvana product, 24 of them generic or store brands. Ask your pharmacist whether one is right for you.
Has Hempvana been recalled?
No recall linked to Hempvana products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Hempvana is

Each Hempvana 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.

Trolamine salicylate · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
trolamine salicylate 10%
cream (topical)
Hempvana Pain Relief 22 products, 16 companies DailyMed
trolamine salicylate 10%
lotion (topical)
Hempvana Maximum Strength Pain Relief None listed DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Trolamine salicylate →

Menthol · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
menthol 8 mg/100 mL
gel (topical)
Hempvana Cold As Ice Pain Relief, Hempvana Cold as Ice Gel None listed DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Menthol →

Lidocaine · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
lidocaine 4%
lotion (topical)
Hempvana Ultra Strength Pain Relief 2 products, 2 companies DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Lidocaine →

FDA approval

Hempvana 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 Hempvana

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

  • Telebrands Corp5 products

Recalls

No recall linked to Hempvana 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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