NOVOMINSYRUP
NOVOMINSYRUP is an FDA drug label for the active ingredient CAFFEINE ANHYDROUS, MECLIZINE HYDROCHLORIDE HYDRATE, PYRIDOXINE HYDROCHLORIDE manufactured by Lydia Co., Ltd. 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 20230123.
- Generic name
- CAFFEINE ANHYDROUS, MECLIZINE HYDROCHLORIDE HYDRATE, PYRIDOXINE HYDROCHLORIDE
- Manufacturer
- Lydia Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 72988-0034
- Application
- N/A
- Label effective
- 20230123
About this product
NOVOMINSYRUP is an FDA-registered drug product whose active ingredient is CAFFEINE ANHYDROUS, MECLIZINE HYDROCHLORIDE HYDRATE, PYRIDOXINE HYDROCHLORIDE. It is labelled by Lydia Co., Ltd. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 72988-0034, label effective 20230123. 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 CAFFEINE ANHYDROUS, MECLIZINE HYDROCHLORIDE HYDRATE, PYRIDOXINE HYDROCHLORIDE are most often described in connection with: years age, older pack, boarding children, ask doctor. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
■ adult and children 15 years of age and older: 1 pack 30 minutes before boarding. ■ children under 15 years of age: ask a doctor
Dosage & Administration
for oral use
Warnings
Ask a doctor before use if you have taking a prescription drug. When using this product ■ Do not take more than 3 pack in 24 hours ■ If you take an additional dose, take it after 4 hours or more Keep out of reach of children
Frequently asked questions
What is NOVOMINSYRUP used for?
■ adult and children 15 years of age and older: 1 pack 30 minutes before boarding. ■ children under 15 years of age: ask a doctor
Who makes NOVOMINSYRUP?
Lydia Co., Ltd. is the labeler of record for NOVOMINSYRUP.
What form does NOVOMINSYRUP 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 NOVOMINSYRUP 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 NOVOMINSYRUP 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.