ISOMETHEPTENE-DICHLORAL-APAP ORAL- isometheptene mucate, dichloralphenazone, and acetaminophen capsule 
Method Pharmaceuticals, LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

Isometheptene-Dichloral-APAP Oral Capsules, USP

ISOMETHEPTENE-DICHLORAL-APAP
ORAL CAPSULES, USP

Class IV Controlled Substance Symbol 

Rx only

LIVER WARNING

This product contains acetaminophen. Severe liver damage may occur if a person takes:

  • More than 4,000 mg of acetaminophen in 24 hours
  • With other drugs containing acetaminophen
  • With 3 or more alcoholic drinks everyday while using this product.

Description

Each red capsule contains:

Isometheptene Mucate, USP       65 mg
Dichloralphenazone, USP       100 mg
Acetaminophen, USP       325 mg

Isometheptene Mucate is a white crystalline powder having a characteristic aromatic odor and bitter taste. It is an unsaturated aliphatic amine with sympathomimetic properties. Its molecular weight is 492.65 and it has the following structural formula:

The structural formula of Isometheptene Mucate.

Acetaminophen, a non-salicylate, occurs as a white, odorless, crystalline powder, possessing a slightly bitter taste. Its molecular weight is 151.16 and it has the following structural formula:

The structural formula of Acetaminophen.

Dichloralphenazone is a white, microcrystalline powder, with slight odor and tastes saline at first, becoming acrid. It is a mild sedative. Its molecular weight is 519.07 and it has the following structural formula:

The structural formula of Dichloralphenazone.

The inactive ingredients are: FD&C Blue #1, Gelatin, Magnesium Stearate, FD&C Red #40, Colloidal Silicon Dioxide, Talc, Titanium Dioxide.

CLINICAL PHARMACOLOGY

Isometheptene Mucate, a sympathomimetic amine, acts by constricting dilated cranial and cerebral arterioles, thus reducing the stimuli that lead to vascular headaches. Dichloralphenazone, a mild sedative, reduces the patient’s emotional reaction to the pain of both vascular and tension headaches. Acetaminophen raises the threshold to painful stimuli, thus exerting an analgesic effect against all types of headaches.

INDICATIONS AND USAGE

For relief of tension and vascular headaches.

 Based on a review of this drug (isometheptene mucate) by the National Academy of Sciences-National Research Council and/or other information, FDA has classified the other indication as “possibly” effective in the treatment of migraine headache. Final classification of the less-than-effective indication requires further investigation.

CONTRAINDICATIONS

ISOMETHEPTENE-DICHLORAL-APAP ORAL CAPSULES, USP is contraindicated in:

• Hypersensitivity or intolerance to any component of this product
• Cardiovascular or cerebrovascular insufficiency, including recent myocardial infarction or stroke
• Glaucoma       • Organic heart disease
• Severe cases of renal disease       • Peripheral vascular disease
• Hypertension       • Hepatic disease

PRECAUTIONS

Caution should be observed in hypertension, peripheral vascular disease and after recent cardiovascular attacks.

This drug may make you dizzy or drowsy. Do not drive, use machinery, or do any activity that requires alertness until you are sure you can perform such activities safely. Avoid alcoholic beverages. Remember that alcohol may be a cause of headaches.

DRUG INTERACTIONS

This drug should not be used with the following medications because very serious interactions may occur: sodium oxybate.

Avoid MAO inhibitors (isocarboxazid, linezolid, methylene blue, moclobemide, phenelzine, procarbazine, rasagiline, selegiline, or tranylcypromine) within 2 weeks before, during, and after treatment with this medication. In some cases a serious (possibly fatal) drug interaction may occur.

Consider drugs that cause drowsiness such as: certain antihistamines (e.g., diphenhydramine), anti-seizure drugs (e.g., carbamazepine, phenytoin), medicine for sleep or anxiety (e.g., alprazolam, diazepam, zolpidem), muscle relaxants (e.g., cyclobenzaprine), narcotic pain relievers (e.g., codeine), psychiatric medicines (e.g., chlorpromazine, risperidone, trazodone).

This medication may interfere with certain laboratory tests (including certain urine glucose tests, urine catecholamine levels, urine 5-HIAA levels), possibly causing false test results.

PREGNANCY

FDA has not assigned a pregnancy category for acetaminophen, dichloralphenazone, or isometheptene. Acetaminophen is routinely used for short-term pain relief and fever in all stages of pregnancy. Acetaminophen crosses the placenta and is believed to be safe in pregnancy when used intermittently for short durations. No controlled studies have been done to establish the safety of dichloralphenazone or isometheptene or of their combination with acetaminophen. ISOMETHEPTENE-DICHLORAL-APAP ORAL CAPSULES, USP should only be given during pregnancy when need has been clearly established.

NURSING MOTHERS

Acetaminophen is excreted into human milk in small concentrations. Metabolites of dichloralphenazone are excreted into human milk. There are no data on the excretion of isometheptene into human milk. Problems in humans have not been documented.

PEDIATRIC USE

Studies with this medicine have been done only in adult patients, and there is no specific information about its use in children.

GERIATRIC

There is no specific published information comparing use of this combination medicine in the elderly with use in other age groups. Geriatric patients are more likely to have peripheral vascular disease, and are therefore more likely to be adversely affected by peripheral vasoconstriction, than are younger adults. However, isometheptene may be safer for elderly patients than the ergot derivatives used to abort acute vascular headaches. Also, elderly patients are more likely to have age related renal function impairment, which may require caution in patients receiving acetaminophen and isometheptene.

ADVERSE REACTIONS

There is a potential for allergic reactions (e.g., swelling of the face, mouth, and throat, difficulty breathing, itching, or rash). A very serious allergic reaction, called anaphylaxis, to this drug is unlikely, but if it occurs, discontinue the drug and seek immediate medical attention.

Transient dizziness, drowsiness, and nausea may occur. This can usually be eliminated by reducing the dose. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

To report SUSPECTED ADVERSE REACTIONS, contact Method Pharmaceuticals, LLC at (817) 250-3427.

OVERDOSAGE

If overdose is suspected, contact your local poison control center at 1-800-222-1222. Symptoms of overdose may include: restlessness, severe drowsiness/dizziness, low body temperature, fast/slow breathing, fast/slow/irregular heartbeat, unresponsiveness.

DOSAGE AND ADMINISTRATION

Do not exceed the recommended dosage because severe liver damage may occur.

Tell your doctor about all usage of pain relievers.

FOR RELIEF OF MIGRAINE HEADACHE: The usual adult dosage is two capsules at once, followed by one capsule every hour until relieved, up to 5 capsules within a twelve hour period.

FOR RELIEF OF TENSION HEADACHE: The usual adult dosage is one or two capsules every four hours up to 8 capsules a day.

HOW SUPPLIED

Red capsules imprinted with VSP1 in bottles of 100ct, NDC 58657-401-01.

Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F)
[See USP Controlled Room Temperature].

Dispense in a tight, light-resistant container (USP/NF) with a child-resistant closure.

Keep out of reach of children.

All prescription substitutions using this product shall be pursuant to state statutes as applicable. This is not an Orange Book product.

Rx only

Manufactured for:
Method Pharmaceuticals, LLC
Arlington, TX 76006
www.methodpharm.com       Rev. 6/14

PRINCIPAL DISPLAY PANEL

NDC 58657-401-01
Isometheptene-Dichloral-APAP Oral Capsules, USP
65 mg/100 mg/325 mg
Rx ONLY

100 CAPSULES

PRINCIPAL DISPLAY PANEL NDC 58657-401-01 Isometheptene-Dichloral- APAP Oral Capsules, USP 65 mg/100 mg/325 mg Rx ONLY 100 CAPSULES
ISOMETHEPTENE-DICHLORAL-APAP  ORAL
isometheptene mucate, dichloralphenazone, and acetaminophen capsule
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:58657-401
Route of AdministrationORALDEA ScheduleCIV    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOMETHEPTENE MUCATE (UNII: 8O120FDS6P) (ISOMETHEPTENE - UNII:Y7L24THH6T) ISOMETHEPTENE MUCATE65 mg
DICHLORALPHENAZONE (UNII: YYX637R279) (CHLORAL HYDRATE - UNII:418M5916WG) DICHLORALPHENAZONE100 mg
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GELATIN (UNII: 2G86QN327L)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorREDScoreno score
ShapeCAPSULESize21mm
FlavorImprint Code VSP1
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58657-401-01100 in 1 BOTTLE; Type 0: Not a Combination Product09/04/201411/20/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER09/04/201411/20/2017
Labeler - Method Pharmaceuticals, LLC (060216698)

Revised: 11/2017
 
Method Pharmaceuticals, LLC