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Brand-name over-the-counter medicine

Flonase Sensimist Allergy

Generic names: Fluticasone furoate · Fluticasone propionate · Acetaminophen, chlorpheniramine and phenylephrine

FDA application holder: Haleon US Holdings

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 Flonase Sensimist Allergy?
Flonase Sensimist Allergy is a brand name of Fluticasone furoate, Fluticasone propionate and Acetaminophen, chlorpheniramine and phenylephrine, an over-the-counter medicine. The FDA NDC Directory lists 7 Flonase Sensimist Allergy products in 3 strengths and forms.
Who makes Flonase Sensimist Allergy?
Haleon US Holdings holds the FDA application for Flonase Sensimist Allergy (NDA022051, approved April 27, 2007). 1 other company (repackagers or distributors) also list Flonase Sensimist Allergy products.
Is there a generic or store brand of Flonase Sensimist Allergy?
Yes. The FDA NDC Directory lists 83 other products with the same active ingredients, strength and form as a Flonase Sensimist Allergy product, 83 of them generic or store brands. Ask your pharmacist whether one is right for you.
Has Flonase Sensimist Allergy been recalled?
No recall linked to Flonase Sensimist Allergy products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Flonase Sensimist Allergy is

Each Flonase Sensimist Allergy 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.

Fluticasone furoate · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
fluticasone furoate 27.5 ug
spray, metered (nasal)
Flonase Sensimist Allergy Relief None listed DailyMed

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

Fluticasone propionate · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
fluticasone propionate 50 ug
spray, metered (nasal)
Childrens Flonase Allergy Relief, Flonase Allergy Relief 73 products, 49 companies DailyMed

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

Acetaminophen, chlorpheniramine and phenylephrine · over-the-counter medicine

Strength and formProduct namesSame medicine, other namesLabel
acetaminophen 325 mg · chlorpheniramine maleate 2 mg · phenylephrine hydrochloride 5 mg
tablet (oral)
FLONASE Headache and Allergy Relief 10 products, 6 companies DailyMed

Its page quotes the Drug Facts label and lists every brand and store brand: Acetaminophen, chlorpheniramine and phenylephrine →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Flonase Sensimist Allergy products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA022051Haleon US HoldingsApril 27, 20074
NDA205434Haleon US HoldingsJuly 23, 20142

Companies that list Flonase Sensimist Allergy

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

Recalls

No recall linked to Flonase Sensimist Allergy 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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