Super-Potent class 1 efficacy1,2

For patients who require a hydrating lotion formulation3

ULTRAVATE® Lotion (halobetasol propionate, 0.05%) provides the hydrating benefits of a cream3

Proven hydration vs a cream formulation3

4
hours
Significantly greater skin surface hydration vs a cream up to 4 hours post-application
6
hours
Matches the hydration of a cream at 6 hours post-application

In the same study, ULTRAVATE® Lotion demonstrated no statistically significant differences in transepidermal water loss compared to a cream formulation.3

Formulated with hydrating emollients to increase and maintain skin moisturization1,3

ULTRAVATE® Lotion hydrating ingredients1,4:

  • Halobetasol propionate, 0.05%
  • Diisopropyl adipate
  • Octyldodecanol
  • Ceteth-20
  • Poloxamer 407
  • Cetyl alcohol
  • Stearyl alcohol
  • Propylparaben
  • Butylparaben
  • Propylene glycol
  • Glycerin
  • Carbomer homopolymer
  • Sodium hydroxide
  • Water
See Tolerability Data
References: 1. ULTRAVATE® Lotion [prescribing information]. Cranbury, NJ: Sun Pharmaceutical Industries, Inc.; 2017. 2. National Psoriasis Foundation. Topical steroid potency chart. https://www.psoriasis.org/about-psoriasis/treatments/topicals/steroids/ potency-chart. Accessed October 31, 2019. 3. Grove G, Zerweck C, Houser T, et al. Occlusivity and moisturization potential of a new lotion formulation of halobetasol propionate, 0.05%. Poster presented at: 74th Annual Meeting of the American Academy of Dermatology; March 4-8, 2016; Washington, DC. 4. EWG’s Skin Deep® Database. Environmental Working Group web site. https://www.ewg.org/skindeep/ingredients/701990-DIISOPROPYL_ADIPATE. Accessed October 30, 2019.
INDICATIONS AND USAGE

ULTRAVATE (halobetasol propionate) Lotion is a corticosteroid indicated for the topical treatment of plaque psoriasis in patients 18 years of age and older.

IMPORTANT SAFETY INFORMATION

Effects on Endocrine System: Reversible hypothalamic-pituitary-adrenal (HPA) axis suppression may occur, with the potential for glucocorticosteroid insufficiency during or after treatment. Systemic effects of topical corticosteroids may also include Cushing’s syndrome, hyperglycemia, and glucosuria. Systemic absorption may require evaluation for HPA axis suppression. Use of potent corticosteroids on large areas, for prolonged durations, under occlusive dressings, or on an altered skin barrier may increase systemic exposure. Children may be more susceptible to systemic toxicity when treated with topical steroids.

Local Adverse Reactions: Local adverse reactions with topical steroids may include atrophy, striae, telangiectasias, burning, itching, irritation, dryness, folliculitis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, secondary infection and miliaria. These may be more likely to occur with occlusive use, prolonged use or more potent corticosteroids, including ULTRAVATE.

Concomitant Skin Infections: Use an appropriate antimicrobial agent if a skin infection is present or develops.

Allergic Contact Dermatitis: Discontinue ULTRAVATE Lotion if allergic contact dermatitis is established.
In clinical trials the most common adverse reactions (≥1%) were telangiectasia, application site atrophy, and headache.

Please see the Full Prescribing Information for complete prescribing details.