HomeNDC LookupIngredientsFluocinonide › 70710-1284-03
Fluocinonide .5 mg/mL Solution, 60 mL — NDC 70710-1284-03 package photo

Fluocinonide .5 mg/mL Solution, 60 mL

by Zydus Pharmaceuticals USA Inc. · 60 mL in 1 BOTTLE (70710-1284-3)
NDC 70710-1284-03
🏷️ FDA NDC (as labeled) 70710-1284-3 billing pads the package segment with a zero
This package
Contains60 mL Cost per mL$0.1985 NADAC Per package$11.91 / 60 ml Pack sizes2 compare ↓
Also priced by: Medicaid pays $0.3767/unit · Part D plans $0.4094/unit — full pricing hub ↓
Also comes in: 20 ml 70710-1284-08
Rx only Generic On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Other active recalls for Fluocinonide (different manufacturers) — 3 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 25, 2026 — Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing. (SUN PHARMACEUTICAL INDUSTRIES INC) · FDA recall D-0476-2026
Class II · Mar 25, 2026 — Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing. (SUN PHARMACEUTICAL INDUSTRIES INC) · FDA recall D-0477-2026
Class II · Mar 25, 2026 — Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing. (SUN PHARMACEUTICAL INDUSTRIES INC) · FDA recall D-0475-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 70710-1284-3
Product NDC 70710-1284
11-digit billing NDC 70710128403
NCPDP billing unit ML — per mL (volume)
RxCUI 310364
UNII 2W4A77YPAN
UPC 0370710128432
Application # ANDA208948
SPL Set ID 73315c87-4e55-41ea-883b-23d504c1b10d
Established class (EPC) Corticosteroid
Mechanism of action Corticosteroid Hormone Receptor Agonists
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-11-01
Route TOPICAL
Dosage form SOLUTION
Substance FLUOCINONIDE
GPI-14 90550060002005
GPI class Fluocinonide
GCN Seq No 007618
GCN 31401
HICL code 003318
Ingredient (HICL) Fluocinonide
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q5
Therapeutic class — intermediate (HIC2) Agents Acting Principally On The Skin
HIC3 code Q5P
Therapeutic class — specific (HIC3) Topical Anti-Inflammatory Steroidal
AHFS code 84:06.08.00
AHFS class Corticosteroids (Skin, Mucous Membrane)
FDB label name FLUOCINONIDE 0.05% SOLUTION
FDB brand name Fluocinonide
Legend status F — Federal legend — prescription drug or device
TE code (Orange Book) AT · RLD · RS
Why two NDCs? The FDA registers this code as 70710-1284-3 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 70710-1284-03. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏷️ RxNorm drug class

This medicine belongs to the Corticosteroid class.

Pharmacologic class Corticosteroid
Drug family (ATC) Corticosteroids, Corticosteroids, potent (group III)
How it works Corticosteroid Hormone Receptor Agonists
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerZydus Pharmaceuticals USA Inc.
Application holderZYDUS PHARMACEUTICALS USA INC
FDA applicationANDA208948 (ANDA)
Labeler code70710
First marketedNov 2018
Product typeHuman Prescription Drug
Portfolio451 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

Label name FLUOCINONIDE 0.05% SOLUTION Ingredient Fluocinonide
📖 What it is MedlinePlus · NLM

Fluocinolone topical is used to treat the itching, redness, dryness, crusting, scaling, inflammation, and discomfort of various skin conditions, including psoriasis (a skin disease in which red, scaly patches form on some areas of the body and eczema (a skin disease that causes the skin to be dry and itchy and to sometimes develop red, scaly rashes). Fluocinolone is in a class of medications called corticosteroids. It works by activating natural substances in the skin to reduce swelling, redness, and itching.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • Fluocinonide is used to calm inflamed, itchy skin — things like eczema (atopic dermatitis), psoriasis, and other inflammatory skin conditions that respond to steroid treatment. It...
  • What skin problems does fluocinonide actually treat?
  • Use a thin layer — just enough to cover the affected area — and rub it in gently. How often you apply it depends on your product and condition: some people use it once a day, other...
  • That's a really common feeling with skin conditions, but with the 0.1% strength products, treatment beyond 2 consecutive weeks is generally not recommended because of the risk of t...
📖 Read our full Fluocinonide guide →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII P7E6YFV72X
    Diisopropyl adipate is a clear, oily liquid derived from adipic acid. It acts as a plasticizer and solvent in medicines, helping soften coatings and improve how the drug dissolves or spreads in the body.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

5 inactive ingredients listed in the exact product block matched to this NDC.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMedingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly $0.199 $11.91 / 60 ml
Medicaid paysCMS SDUD · 12 mo $0.3767 $22.60 / 60 ml
Medicare drug plans payPart D · Q2 2026 $0.4094 $24.56 / 60 ml
NADAC price history (per mL) — tap or hover for the price & month
Dec 2021 Jul 2022 Dec 2025 Aug 2026 $0.427 $0.199
▼ Down 54% over the last 24 months.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
fluocinonide .5 mg/mL 00168-0134-60 E. 1 bottle $0.199 AT Availability likely
Fluocinonide .5 mg/mL 21922-0001-01 Encube 1 bottle $0.199 AT Availability likely
Fluocinonide .5 mg/mLthis 70710-1284-03 Zydus 60 ml $0.199 AT Availability likely
Fluocinonide .5 mg/mL 70752-0154-05 QUAGEN 1 bottle $0.199 AT Availability likely
Fluocinonide .5 mg/mL 72603-0703-01 NorthStar 1 bottle $0.199 AT Availability likely
Fluocinonide .5 mg/mL 33342-0320-84 Macleods 1 bottle $0.316 AT Availability likely +59%
Fluocinonide .5 mg/mL 43386-0026-02 Lupin 1 bottle $0.316 AT Availability likely +59%
Fluocinonide .5 mg/mL 51672-1273-02 Sun 1 bottle $0.316 AT Availability likely +59%
fluocinonide .5 mg/mL 40032-0026-06 Novel 1 bottle AT FDA listed
Fluocinonide .5 mg/mL 63629-9583-01 Bryant 1 bottle AT FDA listed
Fluocinonide .5 mg/mL 68071-3918-06 NuCare 1 bottle AT FDA listed
Fluocinonide .5 mg/mL 70771-1375-03 Zydus 60 ml AT FDA listed
Fluocinonide .5 mg/mL 71656-0094-20 Saptalis 20 ml AT FDA listed
Fluocinonide .5 mg/mL 72162-1270-06 Bryant 1 bottle AT FDA listed
fluocinonide .5 mg/mL 72162-2146-06 Bryant 1 bottle AT FDA listed
Fluocinonide .5 mg/mL 72162-2490-02 Bryant 1 bottle AT FDA listed
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2018
On the market since
Nov 2018
📍
2026
Currently FDA-listed
8 years listed
🔓
·
Generic on the market
this product is a generic
This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🗺️ Medicaid utilization & spend

📍 This exact package only: Medicaid data is reported per full 11-digit NDC — labeler, product and pack size — so every number here is for 70710-1284-03, not the drug overall. Other pack sizes report separately.
💊 Pharmacy benefit only: These are Medicaid outpatient pharmacy claims, billed by NDC. They exclude the medical benefit — clinic- or hospital-administered drugs billed under HCPCS J-codes — so drugs used mostly that way (e.g. Avastin, Lucentis, Keytruda) can look low or missing here. That’s expected, not an error.
📅 Q1 2025 – Q4 2025 · 4 quarters of data
ⓘ The newest quarter is usually incomplete when first published; states restate recent quarters in later CMS releases, so the latest figures typically revise upward. State coverage-policy changes can also shift quarter-to-quarter totals.
Prescriptions last 4 qtrs
25.5K
Units reimbursed last 4 qtrs
1.6M
Gross reimbursed last 4 qtrs
$598.4K
Avg / prescription
$23.50
Avg / unit
$0.3767
Latest quarter Q4 2025
5.7KRx
Medicaid pays / mL
$0.3767
gross reimbursed
vs
NADAC / mL
$0.1985
acquisition cost
=
Spread
+$0.1782
+90% vs cost
What Medicaid paid per mL (before rebates; includes the pharmacy’s dispensing fee) compared with NADAC — the average price pharmacies pay to buy the drug. A positive spread means Medicaid reimbursed more than the purchase price, before manufacturer rebates.
Fee-for-service vs managed care
55% FFS 45% MCO
Fee-for-service · 13,928 Rx Managed care · 11,533 Rx
State Medicaid map
Alaska: no data reported AK Maine: no data reported ME Washington: 10,560 units · 135 per 100k residents WA Idaho: 6,060 units · 309 per 100k residents ID Montana: no data reported MT North Dakota: no data reported ND Minnesota: 59,070 units · 1,030 per 100k residents MN Wisconsin: 21,720 units · 368 per 100k residents WI Michigan: 34,500 units · 344 per 100k residents MI New York: 161,980 units · 828 per 100k residents NY Vermont: 3,720 units · 575 per 100k residents VT New Hampshire: 5,520 units · 394 per 100k residents NH Oregon: 27,420 units · 648 per 100k residents OR Nevada: 20,200 units · 632 per 100k residents NV Wyoming: no data reported WY South Dakota: no data reported SD Iowa: 15,540 units · 485 per 100k residents IA Illinois: 101,680 units · 810 per 100k residents IL Indiana: 25,920 units · 378 per 100k residents IN Ohio: 120,030 units · 1,018 per 100k residents OH Pennsylvania: 27,980 units · 216 per 100k residents PA New Jersey: 720 units · 7.8 per 100k residents NJ Massachusetts: 26,880 units · 384 per 100k residents MA California: 550,460 units · 1,413 per 100k residents CA Utah: 8,880 units · 260 per 100k residents UT Colorado: 31,620 units · 538 per 100k residents CO Nebraska: no data reported NE Missouri: no data reported MO Kentucky: 23,760 units · 525 per 100k residents KY West Virginia: no data reported WV Virginia: 5,940 units · 68.2 per 100k residents VA Maryland: 28,740 units · 465 per 100k residents MD Connecticut: 3,600 units · 99.5 per 100k residents CT Rhode Island: 5,280 units · 482 per 100k residents RI Arizona: 22,560 units · 304 per 100k residents AZ New Mexico: 13,440 units · 636 per 100k residents NM Kansas: 3,600 units · 122 per 100k residents KS Arkansas: no data reported AR Tennessee: 47,760 units · 670 per 100k residents TN North Carolina: 37,800 units · 349 per 100k residents NC South Carolina: 6,980 units · 130 per 100k residents SC Delaware: no data reported DE Oklahoma: 29,580 units · 730 per 100k residents OK Louisiana: 8,400 units · 184 per 100k residents LA Mississippi: 840 units · 28.6 per 100k residents MS Alabama: 8,640 units · 169 per 100k residents AL Georgia: 32,120 units · 291 per 100k residents GA D.C.: 1,440 units · 212 per 100k residents DC Hawaii: 3,780 units · 263 per 100k residents HI Texas: 19,200 units · 62.9 per 100k residents TX Florida: 24,720 units · 109 per 100k residents FL
Units reimbursed · per 100k residents
7.81,413
gray = no data reported
Colors are per 100,000 residents, so big states don’t automatically dominate. Tap or hover a state for its actual totals.
Tap or hover a state
…for its Medicaid breakdown
🏆 Top states by units · per 100k residents
1 California 1,413 /100k
2 Minnesota 1,030 /100k
3 Ohio 1,018 /100k
4 New York 828 /100k
5 Illinois 810 /100k
6 Oklahoma 730 /100k
7 Tennessee 670 /100k
8 Oregon 648 /100k
National units — by quarter
💵 About the dollar figures: “reimbursed” is what Medicaid paid pharmacies before confidential manufacturer rebates, so the program’s real net cost is lower than these numbers. Fee-for-service and managed-care claims are combined unless split above. Source: CMS State Drug Utilization Data; per-100k rates use 2023 Census population estimates.

💊 Medicaid utilization by pack size

Medicaid (SDUD) totals over the four most recent reported quarters for every package size of this drug — handy when a specific package (e.g. a starter/titration pack) carries little or no Medicaid volume on its own.
60 ml this page70710-1284-03 24,887 Rx · $587,102
20 ml70710-1284-08 No Medicaid data
Drug total (last 4 qtrs): 24,887 Rx · 1,554,160 units · $587,102 gross reimbursed
Tap a pack size to open its page. Source: CMS State Drug Utilization Data, last 4 quarters.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Fluocinonide — the program that covers self-administered drugs. 13 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Fluocinonide. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$6.96M
Claims incl. refills
176.2K
Beneficiaries
135.8K
Spend / beneficiary
$51.22
Spend / claim
$39.49
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

📦 Packaging — all sizes for this product

Package NDCDescription Per unit Per pack Marketing startStatus
70710-1284-03 You're viewing this 60 mL in 1 BOTTLE (70710-1284-3) $0.1985 / mL $11.91 2018-11-01 Active
70710-1284-08 20 mL in 1 BOTTLE (70710-1284-8) 2018-11-01 Active

You're viewing the largest of 2 pack sizes for this product.

In Medicaid, this is the most-dispensed pack of this product — about 100% of fills over the last four reported quarters. See all packs ↓

Pack size FAQ

What quantity is in NDC 70710-1284-03?
NDC 70710-1284-03 contains 60 mL — 60 ml in 1 bottle.
What is the difference between NDC 70710-1284-03 and NDC 70710-1284-08?
Both are Fluocinonide .5 mg/mL Solution — the drug itself is identical. NDC 70710-1284-03 is the 60 mL package, while NDC 70710-1284-08 is the 20 ml package.
What NDC number is used to bill for this package of Fluocinonide .5 mg/mL Solution?
Bill NDC 70710-1284-03 — the 11-digit billing format is 70710128403. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

📄 Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage 22 words

INDICATIONS AND USAGE Fluocinonide topical solution USP, 0.05% is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

⏱️ Dosage and Administration 62 words

DOSAGE AND ADMINISTRATION Fluocinonide topical solution USP, 0.05% is generally applied to the affected area as a thin film from two to four times daily depending on the severity of the condition. Occlusive dressings may be used for the management of psoriasis or recalcitrant conditions. If an infection develops, the use of occlusive dressings should be discontinued and appropriate antimicrobial therapy instituted.

Contraindications 21 words

CONTRAINDICATIONS Topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

🤒 Adverse Reactions 59 words

ADVERSE REACTIONS The following local adverse reactions are reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. These reactions are listed in an approximate decreasing order of occurrence: Burning Hypertrichosis Maceration of the skin Itching Acneiform eruptions Secondary infection Irritation Hypopigmentation Skin atrophy Dryness Perioral dermatitis Striae Folliculitis Allergic contact dermatitis Miliaria

🧒 Pediatric Use 114 words

Pediatric Use Pediatric patients may demonstrate greater susceptibility to topical corticosteroid-induced HPA axis suppression and Cushing's syndrome than mature patients because of a larger skin surface area to body weight ratio. Hypothalamic-pituitary-adrenal (HPA) axis suppression, Cushing's syndrome, and intracranial hypertension have been reported in children receiving topical corticosteroids. Manifestations of adrenal suppression in children include linear growth retardation, delayed weight gain, low plasma cortisol levels, and absence of response to ACTH stimulation.

Manifestations of intracranial hypertension include bulging fontanelles, headaches, and bilateral papilledema. Administration of topical corticosteroids to children should be limited to the least amount compatible with an effective therapeutic regimen. Chronic corticosteroid therapy may interfere with the growth and development of children.

🆘 Overdosage 17 words

OVERDOSAGE Topically applied corticosteroids can be absorbed in sufficient amounts to produce systemic effects. (See PRECAUTIONS .)

🧬 Clinical Pharmacology 210 words

CLINICAL PHARMACOLOGY Topical corticosteroids share anti-inflammatory, anti-pruritic and vasoconstrictive actions. The mechanism of anti-inflammatory activity of the topical corticosteroids is unclear. Various laboratory methods, including vasoconstrictor assays, are used to compare and predict potencies and/or clinical efficacies of the topical corticosteroids.

There is some evidence to suggest that a recognizable correlation exists between vasoconstrictor potency and therapeutic efficacy in man. Pharmacokinetics The extent of percutaneous absorption of topical corticosteroids is determined by many factors including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings. A significantly greater amount of fluocinonide is absorbed from the solution than from the cream or gel formulations.

Topical corticosteroids can be absorbed from normal intact skin. Inflammation and/or other disease processes in the skin increase percutaneous absorption. Occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids.

Thus, occlusive dressings may be a valuable therapeutic adjunct for treatment of resistant dermatoses. (See DOSAGE AND ADMINISTRATION .) Once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids. Corticosteroids are bound to plasma proteins in varying degrees.

Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. Some of the topical corticosteroids and their metabolites are also excreted into the bile.

📦 How Supplied / Storage and Handling 77 words

HOW SUPPLIED Fluocinonide Topical Solution USP, 0.05% is clear solution free from particulate matter and is supplied as: NDC 70710-1284-8 in bottle of 20 mL NDC 70710-1284-3 in bottle of 60 mL Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Avoid excessive heat, above 40°C (104°F). Call your doctor for medical advice about side effects.

You may report side effects to FDA at 1-800-FDA-1088. Please address medical inquiries to, ([email protected]) Tel.: 1-877-993-8779.

📋 Description 125 words

DESCRIPTION Fluocinonide topical solution USP, 0.05% is intended for topical administration. The active component is the corticosteroid fluocinonide, which is the 21-acetate ester of fluocinolone acetonide and has the chemical name pregna-1,4 -diene-3,20 -dione,21-(acetyloxy)-6 ,9 -difluoro -11-hydro xy-16 ,17-[(1- methylethylidene)bis(oxy)]-,(6 α, 11β, 16 α)-. It has the following chemical structure: Fluocinonide, USP is white or almost white microcrystalline powder.

It is practically insoluble in water, very slightly soluble in ether, slightly soluble in ethanol, methanol and dioxane, sparingly soluble in acetone and chloroform. Fluocinonide topical solution USP, 0.05% contains fluocinonide USP, 0.5 mg/mL in a solution of citric acid monohydrate, dehydrated alcohol (35%), diisopropyl adipate, propylene glycol and purified water. In this formulation, the active ingredient is totally in solution.

Fluocinonide topical solution USP, 0.5%

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.