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Prescription medicine · generic available

Halcinonide

Drug class: Corticosteroid

The FDA’s “Established Pharmacologic Class”: the group of medicines that work in a similar way.

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

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 Halcinonide used for?
The FDA-approved label (Halog, Genus Lifesciences Inc., January 15, 2026) says: “HALOG (Halcinonide Cream, USP) 0.1% is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Halcinonide have a boxed warning?
No. None of the 7 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Halcinonide?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Halcinonide been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Halcinonide?
5 companies list prescription products of Halcinonide in the FDA NDC Directory, including Genus Lifesciences Inc., Sun Pharmaceutical Industries, Inc. and INA Pharmaceutics Inc.

What Halcinonide is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

HALOG (Halcinonide Cream, USP) 0.1% is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

— FDA label: Halog, Genus Lifesciences Inc., effective January 15, 2026. Read the full label on DailyMed →

The FDA has 7 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

The label quoted above has no boxed warning.

0 of 7 FDA labels for this medicine have a boxed warning.

Forms and how it is given

Dosage formsCream · Solution
RouteTopical
Prescription products7 in the FDA NDC Directory
Brand namesHalog

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Halcinonide, by strength and form
Strength and formGeneric or brandPharmacies pay
halcinonide 1 mg/mL
solution
Generic $6.08 per mL

NADAC list of November 4, 2026; these prices took effect on March 18, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
Brand and biologic applications
ApplicationSponsorApprovedLater changes approved
NDA017556
HALOG
Sun Pharm Inds IncNovember 27, 1974 28, latest April 2, 2014
2014: Manufacturing (CMC) · 2009: Manufacturing (CMC) · 2004: Labeling
NDA017823
HALOG
Sun Pharm Inds IncMay 4, 1977 22, latest March 18, 2020
2020: Manufacturing (CMC) · 2004: Labeling · 1996: Manufacturing (CMC)

Generic approvals (2)

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

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

Official identifiers

RxCUI (RxNorm)103467, 206546, 206550, 310669
SPL set ID of the quoted label484c3224-edd1-db3e-e063-6294a90abc25
FDA labels (SPL)7
FDA applicationsNDA017556, NDA017823, 2 ANDA
Active ingredients (FDA)HALCINONIDE

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Halog, Genus Lifesciences Inc., effective January 15, 2026; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (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. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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