NOCOLD-F
NOCOLD-F is an FDA drug label for the active ingredient ACETAMINOPHENE. CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE 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 20211113.
- Generic name
- ACETAMINOPHENE. CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE
- Manufacturer
- Lydia Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 72988-0027
- Application
- N/A
- Label effective
- 20211113
About this product
NOCOLD-F is an FDA-registered drug product whose active ingredient is ACETAMINOPHENE. CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE. It is labelled by Lydia Co., Ltd. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 72988-0027, label effective 20211113. 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 ACETAMINOPHENE. CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE are most often described in connection with: children years, take bottle, session times, 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 16 years and over: take 1 bottle per session 3 times a day after meal children 11 to 15 years: take 2/3 bottle once a day children 7 to 10 years: take 1/2 bottle once a day children 3 to 6 years: take 1/3 bottle once a day children 2 years: take 1/4 bottle once a day under 2 years: ask a doctor
Dosage & Administration
For oral use only
Warnings
When using this product Do not use for a period longer than 1 weeks Stop use and ask a doctor if nervousness, dizziness, or sleepness occur. Pain, nasal congestion or cough gets worse or lasts more than 7 days. fever gets worse or lasts more than 3 days New symptoms occur These may be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children, In case of overdose, get medical help or contact a poison control center right away
Frequently asked questions
What is NOCOLD-F used for?
adult and children 16 years and over: take 1 bottle per session 3 times a day after meal children 11 to 15 years: take 2/3 bottle once a day children 7 to 10 years: take 1/2 bottle once a day children 3 to 6 years: take 1/3 bottle once a day children 2 years: take 1/4 bottle once a day under 2 years: ask a doctor
Who makes NOCOLD-F?
Lydia Co., Ltd. is the labeler of record for NOCOLD-F.
What form does NOCOLD-F 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 NOCOLD-F 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 NOCOLD-F 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.