BMNP ALLIUM CEPA

ALLIUM CEPA ORAL HUMAN OTC DRUG

BMNP ALLIUM CEPA is an FDA drug label for the active ingredient ALLIUM CEPA manufactured by Total Operations Management LLC DBA:Bestmade Natural Products Micro 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 20260831.

Generic name
ALLIUM CEPA
Manufacturer
Total Operations Management LLC DBA:Bestmade Natural Products Micro
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
82969-5223
Application
N/A
Label effective
20260831

About this product

BMNP ALLIUM CEPA is an FDA-registered drug product whose active ingredient is ALLIUM CEPA. It is labelled by Total Operations Management LLC DBA:Bestmade Natural Products Micro taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 82969-5223, label effective 20260831. It is one of 5 FDA drug label records sharing the active ingredient ALLIUM CEPA. 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 ALLIUM CEPA are most often described in connection with: helps temporarily, relieve watery, nasal discharge, eye irritation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ALLIUM CEPA 30C

Indications & Usage

Helps temporarily relieve: watery nasal discharge, eye irritation, sneezing, nasal irritation

Dosage & Administration

Use as directed. Take with water, 3-4 times daily. Ages 12 and older: 2 pellets. Ages 3 to 11: 1 pellet. Ages below 3: consult your doctor.

Warnings

Keep out of reach of children. If pregnant or breastfeeding, ask a health professional before use. Stop use and ask a doctor if symptoms persist or worsen. If you have severe symptoms, consult a doctor before use.

More products with the same ingredient

ALLIUM CEPA

ALLIUM CEPA

Rxhomeo Private Limited d.b.a. Rxhomeo, Inc View label

Allium Cepa

True Botanica, LLC View label

Allium Cepa

True Botanica, LLC View label

Allium Cepa

OHM PHARMA INC. View label

How products containing ALLIUM CEPA compare

FDA lists 5 drug label records with ALLIUM CEPA as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — True Botanica, LLC 2
— — OHM PHARMA INC. 1
— — Rxhomeo Private Limited d.b.a. Rxhomeo, Inc 1
— — Total Operations Management LLC DBA:Bestmade Natural Products Micro 1
— — — —

Frequently asked questions

What is BMNP ALLIUM CEPA used for?
Helps temporarily relieve: watery nasal discharge, eye irritation, sneezing, nasal irritation

Who makes BMNP ALLIUM CEPA?
Total Operations Management LLC DBA:Bestmade Natural Products Micro is the labeler of record for BMNP ALLIUM CEPA. 5 FDA label records share the active ingredient ALLIUM CEPA, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does BMNP ALLIUM CEPA 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 BMNP ALLIUM CEPA 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.

Are there other products containing ALLIUM CEPA?
Yes. 5 FDA drug label records list ALLIUM CEPA as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has BMNP ALLIUM CEPA 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.