Anxiolix
Anxiolix is an FDA drug label for the active ingredient ARSENICUM ALBUM ,SCUTELLARIA LATERIFLORA,PHOSPHORUS,LACHESIS MUTUS,PULSATILLA,PASSIFLORA INCARNATA,ACONITE,VALERIANA OFFICINALIS,CALCAREA CARBONICA,IGNATIA AMARA manufactured by White Manufacturing Inc. DBA Micro West administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20210121.
- Generic name
- ARSENICUM ALBUM ,SCUTELLARIA LATERIFLORA,PHOSPHORUS,LACHESIS MUTUS,PULSATILLA,PASSIFLORA INCARNATA,ACONITE,VALERIANA OFFICINALIS,CALCAREA CARBONICA,IGNATIA AMARA
- Manufacturer
- White Manufacturing Inc. DBA Micro West
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 61657-0006
- Application
- N/A
- Label effective
- 20210121
About this product
Anxiolix is an FDA-registered drug product whose active ingredient is ARSENICUM ALBUM ,SCUTELLARIA LATERIFLORA,PHOSPHORUS,LACHESIS MUTUS,PULSATILLA,PASSIFLORA INCARNATA,ACONITE,VALERIANA OFFICINALIS,CALCAREA CARBONICA,IGNATIA AMARA. It is labelled by White Manufacturing Inc. DBA Micro West taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 61657-0006, label effective 20210121. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ARSENICUM ALBUM ,SCUTELLARIA LATERIFLORA,PHOSPHORUS,LACHESIS MUTUS,PULSATILLA,PASSIFLORA INCARNATA,ACONITE,VALERIANA OFFICINALIS,CALCAREA CARBONICA,IGNATIA AMARA are most often described in connection with: indications indications, temporary relief, anxiety sleeplessness. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
INDICATIONS INDICATIONS : FOR THE TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS
Dosage & Administration
DIRECTIONS Directions: Take 6 drops orally, 4 times a day. For ages 2 to adult.
Warnings
WARNING WARNING : Stop use and call a doctor if symptoms persist or worsen. If pregnant or breast feeding, consult a healthcare professional before use. Contains alcohol: in case of accidental overdose, consult a poison control center immediately.
Frequently asked questions
What is Anxiolix used for?
INDICATIONS INDICATIONS : FOR THE TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS
Who makes Anxiolix?
White Manufacturing Inc. DBA Micro West is the labeler of record for Anxiolix.
What form does Anxiolix come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Anxiolix prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Anxiolix been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.