Quick answers
- What is Halobetasol propionate and tazarotene used for?
- The FDA-approved label (Duobrii, Bausch Health US, LLC, January 1, 2020) says: “DUOBRII ® (halobetasol propionate and tazarotene) Lotion, 0.01%/0.045% is indicated for the topical treatment of plaque psoriasis in adults. DUOBRII Lotion is a combination of halobetasol propionate and tazarotene indicated for the topical treatment of plaque psoriasis in adults.” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Halobetasol propionate and tazarotene have a boxed warning?
- No. None of the 1 FDA labels we found for this medicine has a boxed warning.
- Is there a shortage of Halobetasol propionate and tazarotene?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Halobetasol propionate and tazarotene been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Halobetasol propionate and tazarotene?
- 1 company lists prescription products of Halobetasol propionate and tazarotene in the FDA NDC Directory, including Bausch Health US, LLC.
What Halobetasol propionate and tazarotene is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
DUOBRII ® (halobetasol propionate and tazarotene) Lotion, 0.01%/0.045% is indicated for the topical treatment of plaque psoriasis in adults. DUOBRII Lotion is a combination of halobetasol propionate and tazarotene indicated for the topical treatment of plaque psoriasis in adults.
— FDA label: Duobrii, Bausch Health US, LLC, effective January 1, 2020. Read the full label on DailyMed →
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.
Forms and how it is given
| Dosage forms | Lotion |
|---|---|
| Route | Topical |
| Prescription products | 1 in the FDA NDC Directory |
| Brand names | Duobrii |
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.
- Bausch Health US, LLC1 product
FDA approval history
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Sponsor | Approved | Later changes approved |
|---|---|---|---|
| NDA209354 DUOBRII | Bausch | April 25, 2019 | — |
Shortage status
The FDA drug shortage list does not show these products.
Recalls
No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.
Official identifiers
| RxCUI (RxNorm) | 2166089, 2166094 |
|---|---|
| SPL set ID of the quoted label | b3f0cdc0-69fd-43d1-baf2-d776a3a20715 |
| FDA labels (SPL) | 1 |
| FDA applications | NDA209354 |
| Active ingredients (FDA) | HALOBETASOL PROPIONATE / TAZAROTENE |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Duobrii, Bausch Health US, LLC, effective January 1, 2020; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- 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 →