NDC 0187-5400 Jublia

Efinaconazole

NDC Product Code 0187-5400

NDC CODE: 0187-5400

Proprietary Name: Jublia What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Efinaconazole What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used to treat toenail infection caused by fungus. It works by stopping the growth of certain types of fungus. Efinaconazole belongs to a class of drugs known as azole antifungals. This medication treats only fungal infections. It will not work for other types of infection, such as those caused by bacteria. Unnecessary use or overuse of any drug used to treat infection can lead to its decreased effectiveness.

NDC Code Structure

NDC 0187-5400-02

Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON > 2 mL in 1 BOTTLE, WITH APPLICATOR

NDC 0187-5400-04

Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON > 4 mL in 1 BOTTLE, WITH APPLICATOR

NDC 0187-5400-08

Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON > 8 mL in 1 BOTTLE, WITH APPLICATOR

NDC Product Information

Jublia with NDC 0187-5400 is a a human prescription drug product labeled by Bausch Health Us Llc. The generic name of Jublia is efinaconazole. The product's dosage form is solution and is administered via topical form.

Labeler Name: Bausch Health Us Llc

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

Product Type: Human Prescription Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Jublia Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • EFINACONAZOLE 100 mg/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
  • CYCLOMETHICONE (UNII: NMQ347994Z)
  • DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Azole Antifungal - [EPC] (Established Pharmacologic Class)
  • Azoles - [CS]

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Bausch Health Us Llc
Labeler Code: 0187
FDA Application Number: NDA203567 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: NDA - A product marketed under an approved New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 06-06-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

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Information for Patients

Efinaconazole Topical

Efinaconazole Topical is pronounced as (ef'' in a kon' a zole)

Why is efinaconazole topical medication prescribed?
Efinaconazole topical solution is used to treat fungal toenail infections (infections that may cause nail discoloration, splitting, or pain). Efinaconazole topical soluti...
[Read More]

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Jublia Product Label Images

Jublia Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

1 Indications And Usage

JUBLIA (efinaconazole) topical solution, 10% is an azole antifungal indicated for the topical treatment of onychomycosis of the toenail(s) due to Trichophyton rubrum and Trichophyton mentagrophytes.

2 Dosage And Administration

Apply JUBLIA to affected toenails once daily for 48 weeks, using the integrated flow-through brush applicator. When applying JUBLIA, ensure the toenail, the toenail folds, toenail bed, hyponychium, and the undersurface of the toenail plate, are completely covered.JUBLIA is for topical use only and not for oral, ophthalmic, or intravaginal use.

3 Dosage Forms And Strengths

JUBLIA (efinaconazole) topical solution, 10% contains 100 mg of efinaconazole in each gram of clear, colorless to pale yellow solution.

4 Contraindications

None.

6.1 Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.In two clinical trials, 1227 subjects were treated with JUBLIA, 1161 for at least 24 weeks and 780 for 48 weeks. Adverse reactions reported within 48 weeks of treatment and in at least 1% of subjects treated with JUBLIA and those reported in subjects treated with the vehicle are presented in Table 1.Table 1: Adverse Reactions Reported by at Least 1% of Subjects Treated for up to 48 WeeksAdverse Event, n (%)JUBLIAN = 1227VehicleN = 413Ingrown toenail28 (2.3%)3 (0.7%)Application site dermatitis27 (2.2%)1 (0.2%)Application site vesicles20 (1.6%)0 (0.0%)Application site pain13 (1.1%)1 (0.2%)

7 Drug Interactions

In vitro studies have shown that JUBLIA, at therapeutic concentrations, neither inhibits nor induces cytochrome P450 (CYP450) enzymes.

8.1 Pregnancy

Pregnancy Category CThere are no adequate and well-controlled studies with JUBLIA in pregnant women. JUBLIA should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.Systemic embryofetal development studies were conducted in rats and rabbits. Subcutaneous doses of 2, 10 and 50 mg/kg/day efinaconazole were administered during the period of organogenesis (gestational days 6-16) to pregnant female rats. In the presence of maternal toxicity, embryofetal toxicity (increased embryofetal deaths, decreased number of live fetuses, and placental effects) was noted at 50 mg/kg/day [559 times the Maximum Recommended Human Dose (MRHD) based on Area Under the Curve (AUC) comparisons]. No embryofetal toxicity was noted at 10 mg/kg/day (112 times the MRHD based on AUC comparisons). No malformations were observed at 50 mg/kg/day (559 times the MRHD based on AUC comparisons).Subcutaneous doses of 1, 5, and 10 mg/kg/day efinaconazole were administered during the period of organogenesis (gestational days 6-19) to pregnant female rabbits. In the presence of maternal toxicity, there was no embryofetal toxicity or malformations at 10 mg/kg/day (154 times the MRHD based on AUC comparisons).In a pre- and post-natal development study in rats, subcutaneous doses of 1, 5 and 25 mg/kg/day efinaconazole were administered from the beginning of organogenesis (gestation day 6) through the end of lactation (lactation day 20). In the presence of maternal toxicity, embryofetal toxicity (increased pre-natal pup mortality, reduced live litter sizes and increased post-natal pup mortality) was noted at 25 mg/kg/day. No embryofetal toxicity was noted at 5 mg/kg/day (17 times the MRHD based on AUC comparisons). No effects on post-natal development were noted at 25 mg/kg/day (89 times the MRHD based on AUC comparisons).

8.3 Nursing Mothers

It is not known whether efinaconazole is excreted in human milk. After repeated subcutaneous administration, efinaconazole was detected in milk of nursing rats. Because many drugs are excreted in human milk, caution should be exercised when JUBLIA is administered to nursing women.

8.4 Pediatric Use

Safety and effectiveness of JUBLIA in pediatric subjects have not been established.

8.5 Geriatric Use

Of the total number of subjects in clinical trials of JUBLIA, 11.3% were 65 and over, while none were 75 and over. No overall differences in safety and effectiveness were observed between these subjects and younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and the younger subjects, but greater sensitivity of some older individuals cannot be ruled out.

11 Description

JUBLIA (efinaconazole) topical solution, 10% is a clear colorless to pale yellow solution for topical use. Each gram of JUBLIA contains 100 mg of efinaconazole. Efinaconazole is an azole antifungal with a chemical name of ((2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidin-1-yl)-1-(1H-1,2,4-triazol-1-yl) butan-2-ol). The structural formula for efinaconazole is represented below:JUBLIA contains the following inactive ingredients: alcohol, anhydrous citric acid, butylated hydroxytoluene, C12-15 alkyl lactate, cyclomethicone, diisopropyl adipate, disodium edetate, and purified water.

12.1 Mechanism Of Action

JUBLIA topical solution is an azole antifungal [see Clinical Pharmacology (12.4)].

12.2 Pharmacodynamics

The pharmacodynamics of JUBLIA is unknown.

12.3 Pharmacokinetics

Systemic absorption of efinaconazole in 18 adult subjects with severe onychomycosis was determined after application of JUBLIA once daily for 28 days to patients’ 10 toenails and 0.5 cm adjacent skin. The concentration of efinaconazole in plasma was determined at multiple time points over the course of 24-hour periods on days 1, 14, and 28. Efinaconazole mean ± SD plasma Cmax on Day 28 was 0.67 ± 0.37 ng/mL and the mean ± SD AUC was 12.15 ± 6.91 ng*h/mL. The plasma concentration versus time profile at steady state was generally flat over a 24-hour dosing interval. In a separate study of healthy volunteers, the plasma half-life of efinaconazole following daily applications when applied to all 10 toenails for 7 days was 29.9 hours.Drug InteractionsJUBLIA is considered a non-inhibitor of the CYP450 enzyme family. In in vitro studies using human liver microsomes, efinaconazole did not inhibit CYP1A2, CYP2A6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP2PE1 and CYP3A4 enzyme activities at expected clinical systemic concentrations. In vitro studies in human primary hepatocytes showed that efinaconazole did not induce CYP1A2 or CYP3A4 activities.

12.4 Microbiology

Mechanism of ActionEfinaconazole is an azole antifungal. Efinaconazole inhibits fungal lanosterol 14α-demethylase involved in the biosynthesis of ergosterol, a constituent of fungal cell membranes.Activity In Vitro and In VivoEfinaconazole has been shown to be active against isolates of the following microorganisms, both in vitro and in clinical infections. Efinaconazole exhibits in vitro minimum inhibitory concentrations (MICs) of 0.06 mcg/mL or less against most (≥90%) isolates of the following microorganisms:   Trichophyton rubrum   Trichophyton mentagrophytesMechanism of ResistanceEfinaconazole drug resistance development was studied in vitro against T. mentagrophytes, T. rubrum and C. albicans. Serial passage of fungal cultures in the presence of sub-growth inhibitory concentrations of efinaconazole increased the MIC by up to 4-fold. The clinical significance of these in vitro results is unknown.

13.1 Carcinogenesis, Mutagenesis, Impairment Of Fertility

A 2-year dermal carcinogenicity study in mice was conducted with daily topical administration of 3%, 10% and 30% efinaconazole solution. Severe irritation was noted at the treatment site in all dose groups, which was attributed to the vehicle and confounded the interpretation of skin effects by efinaconazole. The high dose group was terminated at week 34 due to severe skin reactions. No drug-related neoplasms were noted at doses up to 10% efinaconazole solution (248 times the MRHD based on AUC comparisons).Efinaconazole revealed no evidence of mutagenic or clastogenic potential based on the results of two in vitro genotoxicity tests (Ames assay and Chinese hamster lung cell chromosome aberration assay) and one in vivo genotoxicity test (mouse peripheral reticulocyte micronucleus assay).No effects on fertility were observed in male and female rats that were administered subcutaneous doses up to 25 mg/kg/day efinaconazole (279 times the MRHD based on AUC comparisons) prior to and during early pregnancy. Efinaconazole delayed the estrous cycle in females at 25 mg/kg/day but not at 5 mg/kg/day (56 times MRHD based on AUC comparisons).

14 Clinical Studies

  • The safety and efficacy of once daily use of JUBLIA for the treatment of onychomycosis of the toenail were assessed in two 52-week prospective, multi-center, randomized, double-blind clinical trials in patients 18 years and older (18 to 70 years of age) with 20% to 50% clinical involvement of the target toenail, without dermatophytomas or lunula (matrix) involvement. The trials compared 48 weeks of treatment with JUBLIA to the vehicle solution. The Complete Cure rate was assessed at Week 52 (4 weeks after completion of therapy). Complete cure was defined as 0% involvement of the target toenail (no clinical evidence of onychomycosis of the target toenail) in addition to Mycologic Cure, defined as both negative fungal culture and negative KOH. Table 2 lists the efficacy results for trials 1 and 2.  Table 2:Efficacy EndpointsTrial 1Trial 2JUBLIAVehicleJUBLIAVehicleN = 656N = 214N = 580N = 201a Complete cure defined as 0% clinical involvement of the target toenail plus negative KOH and negative culture.b Complete or almost complete cure defined as ≤5% affected target toenail area involved and negative KOH and culture.c Mycologic cure defined as negative KOH and negative culture. Complete Curea11717.8%73.3%8815.2%115.5%Complete or Almost Complete Cureb17326.4%157.0%13623.4%157.5%Mycologic Curec36255.2%3616.8%31053.4%3416.9%

16 How Supplied/Storage And Handling

  • JUBLIA (efinaconazole) topical solution, 10% is a clear, colorless to pale yellow solution supplied in a white plastic bottle with an integrated flow-through brush applicator as follows: •4 mL (NDC 0187-5400-04) •8 mL (NDC 0187-5400-08)

Storage And Handling

  • Storage and Handling Conditions:Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature]. •Solution is flammable; keep away from heat or flame •Protect from freezing •Keep out of the reach of children •Keep bottle tightly closed •Store in upright position

17 Patient Counseling Information

  • Advise the patient to read the FDA-approved patient labeling (Patient Information and Instructions for Use). •JUBLIA is for external use only and is not for ophthalmic, oral, or intravaginal use. It is for use on toenails and immediately adjacent skin only. •Apply JUBLIA once daily to clean dry toenails. Wait for at least 10 minutes after showering, bathing, or washing before applying. •Use JUBLIA only on the affected toenails, as directed by your healthcare provider. •Inform a healthcare professional if the area of application shows signs of persistent irritation (for example, redness, itching, swelling). •The impact of nail polish or other cosmetic nail products on the efficacy of JUBLIA has not been evaluated. •Flammable, avoid use near heat or open flame.

Other

Manufactured for:Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USAby: Valeant Pharmaceuticals International Inc. Laval, Quebec H7L 4A8, CanadaOrManufactured for: Valeant Pharmaceuticals North America LLCBridgewater, NJ 08807 USAby:Kaken Pharmaceutical Co., Ltd.Shizuoka-ken 426-8646, JapanU.S. Patents 7,214,506; 8,039,494; 8,486,978; and 9,302,009 Jublia is a trademark of Valeant PharmaceuticalsInternational, Inc. or its affiliates.© Valeant Pharmaceuticals North America LLCValeant Pharmaceuticals International Inc. PI:Rev. 09/20169462903Kaken Pharmaceutical Co. Ltd PI:Rev. 09/20169391906

Spl Patient Package Insert

  • PATIENT INFORMATIONJUBLIA (joo-blee-uh)(efinaconazole) topical solution, 10%Important information: JUBLIA is for use on toenails and surrounding skin only. Do not use JUBLIA in your mouth, eyes, or vagina.What is JUBLIA?JUBLIA is a prescription medicine used to treat fungal infections of the toenails.It is not known if JUBLIA is safe and effective in children.What should I tell my healthcare provider before using JUBLIA?Before you use JUBLIA, tell your healthcare provider about all your medical conditions, including if you: •are pregnant or plan to become pregnant. It is not known if JUBLIA can harm your unborn baby. •are breastfeeding or plan to breastfeed. It is not known if JUBLIA passes into your breast milk.Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.How should I use JUBLIA?See the “Instructions for Use” at the end of this Patient Information leaflet for detailed information about the right way to use JUBLIA. •Use JUBLIA exactly as your healthcare provider tells you to use it. Apply JUBLIA to your affected toenails 1 time each day. Wait for at least 10 minutes after showering, bathing, or washing before applying JUBLIA. JUBLIA is used for 48 weeks. •It is not known if the use of nail polish or other cosmetic nail products (such as gel nails or acrylic nails) will affect how JUBLIA works.What should I avoid while using JUBLIA? •JUBLIA is flammable. Avoid heat and flame while applying JUBLIA to your toenail.What are the possible side effects of JUBLIA?JUBLIA may cause irritation at the treated site. The most common side effects include: ingrown toenail, redness, itching, swelling, burning or stinging, blisters, and pain. Tell your healthcare provider if you have any side effects that bother you or that do not go away.These are not all the possible side effects of JUBLIA.Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.How should I store JUBLIA? •Store JUBLIA at room temperature, between 68°F to 77°F (20°C to 25°C). Do not freeze JUBLIA. •Keep the bottle tightly closed and store in an upright position. •JUBLIA is flammable. Keep away from heat and flame.Keep JUBLIA and all medicines out of the reach of children.General information about the safe and effective use of JUBLIAMedicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. You can ask your pharmacist or healthcare provider for information about JUBLIA that is written for health professionals. Do not use JUBLIA for a condition for which it was not prescribed. Do not give JUBLIA to other people, even if they have the same condition you have. It may harm them.What are the ingredients in JUBLIA?Active ingredients: efinaconazoleInactive ingredients: alcohol, anhydrous citric acid, butylated hydroxytoluene, C12-15 alkyl lactate, cyclomethicone, diisopropyl adipate, disodium edetate, and purified water.Manufactured for:Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USAby: Valeant Pharmaceuticals International Inc. Laval, Quebec H7L 4A8, CanadaOrManufactured for: Valeant Pharmaceuticals North America LLCBridgewater, NJ 08807 USAby:Kaken Pharmaceutical Co., Ltd.Shizuoka-ken 426-8646, JapanFor more information, call 1-800-321-4576.This Patient Information has been approved by the U.S. Food and Drug Administration.Valeant Pharmaceuticals International Inc. Patient Information:Rev. 09/20169462903Kaken Pharmaceutical Co. Ltd Patient Information:Rev. 09/20169391906Instructions for UseJUBLIA® (joo-blee-uh)(efinaconazole) topical solution, 10%Important information: JUBLIA is for use on toenails and surrounding skin only. Do not use JUBLIA in your mouth, eyes or vagina.Read this Instructions for Use that comes with JUBLIA before you start using it. Talk to your healthcare provider if you have any questions.How to apply JUBLIA:Your toenails should be clean and dry before you apply JUBLIA.Step 1: Remove the cap from the JUBLIA bottle.Step 2: Hold the bottle upside down directly over the affected toenail. By turning the bottle upside down, the entire brush will become moistened with the solution. Apply one drop of JUBLIA onto the toenail. Do not squeeze the bottle, or press or rub the brush firmly against the toenail while applying JUBLIA. Step 3: For the big toenail, also apply a second drop to the end of the toenail using the tip of the brush. If needed, repeat Step 2 to re-wet the brush.Step 4: Use the brush to gently spread JUBLIA around the entire toenail, including the cuticle, folds of the skin next to the sides of the toenail, and underneath the nail.Do not squeeze the bottle, or press or rub the brush firmly against the toenail while spreading JUBLIA with the brush. Step 5: Repeat Steps 2 to 4 to apply JUBLIA to each affected toenail.Step 6: Let JUBLIA dry completely.Step 7: After applying JUBLIA to your affected toenails, place the cap on the bottle and screw it on tightly.Step 8: Wash your hands with soap and water after applying JUBLIA.This Instructions for Use has been approved by the U.S. Food and Drug Administration. Manufactured for:Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USAManufactured by: Valeant Pharmaceuticals International, Inc., Laval, Quebec H7L 4A8, CanadaOrManufactured for: Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USAManufactured by: Kaken Pharmaceutical Co., Ltd., Shizuoka, JapanValeant Pharmaceuticals International Inc. PI and Instructions for Use:Rev. 09/20169462903Kaken Pharmaceutical Co., Ltd. PI and Instructions for Use:Rev. 09/20169391906

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