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Brand-name over-the-counter medicine

Halls

Generic names: Menthol · Pectin

Company: Mondelez Global LLC

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 Halls?
Halls is a brand name of Menthol and Pectin, an over-the-counter medicine. The FDA NDC Directory lists 24 Halls products in 14 strengths and forms.
Who makes Halls?
Mondelez Global LLC lists 24 of the 24 Halls products in the FDA NDC Directory.
Is there a generic or store brand of Halls?
Yes. The FDA NDC Directory lists 214 other products with the same active ingredients, strength and form as a Halls product, 214 of them generic or store brands. Ask your pharmacist whether one is right for you.
Has Halls been recalled?
No recall linked to Halls products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Halls is

Each Halls 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 · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
menthol 1.8 mg
lozenge (oral)
HALLS Honey 2 products, 2 companies DailyMed
menthol 18 mg
lozenge (oral)
HALLS Extra Strong None listed DailyMed
menthol 2.5 mg
lozenge (oral)
Halls Green Apple, Halls Honey Vanilla, Halls Sugar Free Honey Lemon, Halls Sugar Free Watermelon 8 products, 4 companies DailyMed
menthol 2.7 mg
lozenge (oral)
Halls Sugar Free Mentho-Lyptus, Halls Strawberry 13 products, 11 companies DailyMed
menthol 2.9 mg
lozenge (oral)
Halls Sugar Free Cherry None listed DailyMed
menthol 3.2 mg
lozenge (oral)
Halls Strawberry None listed DailyMed
menthol 5.4 mg
lozenge (oral)
Halls MENTHO-LYPTUS, HALLS Mentholyptus 40 products, 27 companies DailyMed
menthol 5.8 mg
lozenge (oral)
Halls Sugar Free Mountain Menthol, Halls Cherry, Halls Sugar Free Black Cherry 65 products, 35 companies DailyMed
menthol 6.4 mg
lozenge (oral)
Halls Mentholyptus None listed DailyMed
menthol 6.8 mg
lozenge (oral)
Halls Cherry None listed DailyMed
menthol 7.5 mg
lozenge (oral)
Halls Honey Lemon 44 products, 32 companies DailyMed
menthol 7.6 mg
lozenge (oral)
Halls Sugar Free Honey Lemon 32 products, 26 companies DailyMed
menthol 8.8 mg
lozenge (oral)
Halls Honey Lemon None listed DailyMed

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

Pectin · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
pectin 7 mg
lozenge (oral)
Halls Breezers Sugar Free Cool Berry 10 products, 6 companies DailyMed

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

FDA approval

Halls 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 Halls

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

  • Mondelez Global LLC24 products

Recalls

No recall linked to Halls 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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