Drugplain

EnilloRing .015 mg/d

Etonogestrel and Ethinyl Estradiol Vaginal · RING · Xiromed, LLC

No Recall HistoryCurrently in Shortage
Plain English

EnilloRing is a ring containing etonogestrel and ethinyl estradiol vaginal at .015 mg/d, taken vaginal. Manufactured by Xiromed, LLC.

Key Facts

Brand Name
EnilloRing
Generic Name
Etonogestrel and Ethinyl Estradiol Vaginal
NDC Code (Product)
70700-156
Manufacturer
Xiromed, LLC
Strength
.015 mg/d
Dosage Form
RING
Route
VAGINAL
Marketing Status
Application #
ANDA211157
Drug Class
Estrogen [EPC]; Progestin [EPC]
Marketing Start
08/15/2023

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

intermenstrual bleeding7 reports
product substitution issue5 reports
product use in unapproved indication4 reports
device physical property issue3 reports
headache3 reports
product prescribing issue3 reports
product quality issue3 reports
vaginal discharge3 reports
device use issue2 reports
dizziness2 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

1 INDICATIONS AND USAGE FOR VAGINAL USE ONLY EnilloRing is indicated for use by females of reproductive age to prevent pregnancy. EnilloRing is an estrogen/progestin combination hormonal contraceptive (CHC) indicated for use by women to prevent pregnancy. ( 1 )

Dosage & Administration

2 DOSAGE AND ADMINISTRATION One EnilloRing is inserted in the vagina. The ring must remain in place continuously for three weeks, followed by a one-week ring-free interval. ( 2 ) 2.1 How to Use EnilloRing To achieve maximum contraceptive effectiveness, EnilloRing must be used as directed [ see Dosage and Administration ( 2.2 )]. One EnilloRing is inserted in the vagina. The ring is to remain in place continuously for three weeks. It is removed for a one-week break, during which a withdrawal bleed usually occurs. A new ring is inserted one week after the last ring was removed. The user can choose the insertion position that is most comfortable to her, for example, standing with one leg up, squatting, or lying down. The ring is to be compressed and inserted into the vagina. An optional alternative is to insert the ring using the applicator for EnilloRing [see Applicator for EnilloRing Instructions for Use ]. The exact position of EnilloRing inside the vagina is not critical for its function. The vaginal ring must be inserted on the appropriate day and left in place for three consecutive weeks. This means that the ring should be removed three weeks later on the same day of the week as

Contraindications

4 CONTRAINDICATIONS EnilloRing is contraindicated in females who are known to have or develop the following conditions: A high risk of arterial or venous thrombotic diseases. Examples include women who are known to: Smoke, if over age 35 [see Boxed Warning and Warnings and Precautions ( 5.1 )] Have deep vein thrombosis or pulmonary embolism, now or in the past [see Warnings and Precautions ( 5.1 )] Have cerebrovascular disease [see Warnings and Precautions ( 5.1 )] Have coronary artery disease [see Warnings and Precautions ( 5.1 )] Have thrombogenic valvular or thrombogenic rhythm diseases of the heart (for example, subacute bacterial endocarditis with valvular disease, or atrial fibrillation) [see Warnings and Precautions ( 5.1 )] Have inherited or acquired hypercoagulopathies [see Warnings and Precautions ( 5.1 )] Have uncontrolled hypertension [see Warnings and Precautions ( 5.5 )] Have diabetes mellitus with vascular disease [see Warnings and Precautions ( 5.9 )] Have headaches with focal neurological symptoms or migraine headaches with aura [see Warnings and Precautions ( 5.10 )] Women over age 35 with any migraine headaches [see Warnings and Precautions ( 5.10 )] Liver tumors

Drug Interactions

7 DRUG INTERACTIONS Consult the labeling of all concurrently-used drugs to obtain further information about interactions with hormonal contraceptives or the potential for enzyme alterations. Drugs or herbal products that induce certain enzymes, such as CYP3A4, may decrease the effectiveness of CHCs or increase breakthrough bleeding. Counsel patients to use a back-up or alternative method of contraception when enzyme inducers are used with CHCs. ( 7 ) 7.1 Effects of Other Drugs on CHCs Substances decreasing the plasma concentrations of CHCs and potentially diminishing the effectiveness of CHCs Drugs or herbal products that induce certain enzymes, including cytochrome P450 3A4 (CYP3A4), may decrease the plasma concentrations of CHCs and potentially diminish the effectiveness of CHCs or increase breakthrough bleeding. Some drugs or herbal products that may decrease the effectiveness of hormonal contraceptives include: phenytoin, barbiturates, carbamazepine, bosentan, felbamate, griseofulvin, oxcarbazepine, rifampicin, topiramate, rifabutin, rufinamide, aprepitant, and products containing St. John's wort. Interactions between CHCs and other drugs may lead to breakthrough bleeding and/o

Adverse Reactions

6 ADVERSE REACTIONS The following serious adverse reactions with the use of CHCs are discussed elsewhere in the labeling. Serious cardiovascular events and stroke [ see Boxed Warning and Warnings and Precautions ( 5.1 ) ] Vascular events [ see Warnings and Precautions ( 5.1 ) ] Liver disease [ see Warnings and Precautions ( 5.3 ) ] Adverse reactions commonly reported by CHC users are: Irregular uterine bleeding Nausea Breast tenderness Headache The most common adverse reactions (≥2%) in clinical trials were: vaginitis, headache (including migraine), mood changes (e.g., depression, mood swings, mood altered, depressed mood, affect lability), device-related events (e.g., expulsion/discomfort/foreign body sensation), nausea/vomiting, vaginal discharge, increased weight, vaginal discomfort, breast pain/discomfort/tenderness, dysmenorrhea, abdominal pain, acne, and decreased libido. ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact Xiromed, LLC at 844-XIROMED (844-947-6633) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a dr

Frequently Asked Questions

What is EnilloRing used for?

EnilloRing contains Etonogestrel and Ethinyl Estradiol Vaginal. It is a ring taken vaginal. Consult your doctor for specific uses.

Is EnilloRing a controlled substance?

EnilloRing is not classified as a controlled substance by the DEA.

What is the generic name for EnilloRing?

The generic name for EnilloRing is Etonogestrel and Ethinyl Estradiol Vaginal. There are 2 other brand versions of Etonogestrel and Ethinyl Estradiol Vaginal.

What is the NDC code for EnilloRing .015 mg/d?

The NDC (National Drug Code) for EnilloRing .015 mg/d is 70700-156, listed by Xiromed, LLC.

Product NDC

70700-156

Package NDC

70700-156-91

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)