BHI Calming
BHI Calming is an FDA drug label for the active ingredient MATRICARIA RECUTITA, ARABICA COFFEE BEAN, HOPS, STRYCHNOS IGNATII SEED, MOSCHUS MOSCHIFERUS MUSK SAC RESIN, STRYCHNOS NUX-VOMICA SEED, PASSIFLORA INCARNATA FLOWERING TOP, SULFUR, VALERIAN, AND VERATRUM ALBUM ROOT manufactured by MediNatura Inc 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 20230802.
- Generic name
- MATRICARIA RECUTITA, ARABICA COFFEE BEAN, HOPS, STRYCHNOS IGNATII SEED, MOSCHUS MOSCHIFERUS MUSK SAC RESIN, STRYCHNOS NUX-VOMICA SEED, PASSIFLORA INCARNATA FLOWERING TOP, SULFUR, VALERIAN, AND VERATRUM ALBUM ROOT
- Manufacturer
- MediNatura Inc
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 62795-1006
- Application
- N/A
- Label effective
- 20230802
About this product
BHI Calming is an FDA-registered drug product whose active ingredient is MATRICARIA RECUTITA, ARABICA COFFEE BEAN, HOPS, STRYCHNOS IGNATII SEED, MOSCHUS MOSCHIFERUS MUSK SAC RESIN, STRYCHNOS NUX-VOMICA SEED, PASSIFLORA INCARNATA FLOWERING TOP, SULFUR, VALERIAN, AND VERATRUM ALBUM ROOT. It is labelled by MediNatura Inc taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 62795-1006, label effective 20230802. 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 MATRICARIA RECUTITA, ARABICA COFFEE BEAN, HOPS, STRYCHNOS IGNATII SEED, MOSCHUS MOSCHIFERUS MUSK SAC RESIN, STRYCHNOS NUX-VOMICA SEED, PASSIFLORA INCARNATA FLOWERING TOP, SULFUR, VALERIAN, AND VERATRUM ALBUM ROOT are most often described in connection with: temporary relief, minor occassional, simple nervous, irritability help. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
USES For the temporary relief of minor occassional simple nervous tension and irritability to help occassional sleeplessness
Dosage & Administration
DIRECTIONS At first sign of symptoms: Adults and children 12 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage. Standard dosage: Adults and children 12 years and older: Take 1-2 tablets every 4 to 6 hours. Do not exceed 12 tablets in 24 hours. For children under 12, consult your health professional. Allow tablets to dissolve completely in the mouth, do not swallow.
Warnings
WARNINGS Do not give to children under 12 years of age. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If sleeplessness or nervous tension persist continuously for more than two weeks, a health professional should be consulted. Insomnia may be a symptom of serious underlying medical illness. Do not use if known sensitivity to BHI Calming or any of its ingredients exists
Frequently asked questions
What is BHI Calming used for?
USES For the temporary relief of minor occassional simple nervous tension and irritability to help occassional sleeplessness
Who makes BHI Calming?
MediNatura Inc is the labeler of record for BHI Calming.
What form does BHI Calming 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 BHI Calming 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 BHI Calming 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.