ClorRelief

ClorRelief is an FDA-registered drug product whose active ingredient is CHLORPHENIRAMINE MALEATE. It is labelled by FERRER MEDICAL INNOVATIONS LLC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 82643-002, application M012, label effective 20260522. It is one of 17 FDA drug label records sharing the active ingredient CHLORPHENIRAMINE MALEATE. 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.

Across FDA labelling, products containing CHLORPHENIRAMINE MALEATE are most often described in connection with: temporarily relieves, symptoms hay, upper respiratory, allergies runny, nose itchy, throat sneezing, watery eyes. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Temporarily relieves symptoms of hay fever or other upper respiratory allergies: runny nose itchy nose or throat sneezing itchy, watery eyes

Directions Adults and children 12 years and over: For each application, spray 4 times every 4 to 6 hours, do not exceed 6 applications in 24 hours. Children 6 to under 12 years of age: Should be supervised in the use of this product. For each application, spray 2 times every 4 to 6 hours. Do not exceed 3 applications in 24 hours. Children 4 to under 6 years of age: Do not use unless directed by a doctor. Children under 4 years of age: Do not use.

Warnings Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers When using this product you may get drowsy avoid alcoholic drinks, sedatives & tranquilizers, may increase drowsiness be careful when driving a motor vehicle or operating machinery excitability may occur, especially in children If pregnant or breastfeeding, ask your doctor before use. Keep out of reach of children Do not use to make a child sleepy. In case of overdose, getmedical help or contact a Poison Control Center right away.

FDA lists 17 drug label records with CHLORPHENIRAMINE MALEATE 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.

What is ClorRelief used for?
Uses Temporarily relieves symptoms of hay fever or other upper respiratory allergies: runny nose itchy nose or throat sneezing itchy, watery eyes

Who makes ClorRelief?
FERRER MEDICAL INNOVATIONS LLC is the labeler of record for ClorRelief. 17 FDA label records share the active ingredient CHLORPHENIRAMINE MALEATE, 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 ClorRelief 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 ClorRelief 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 CHLORPHENIRAMINE MALEATE?
Yes. 17 FDA drug label records list CHLORPHENIRAMINE MALEATE 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 ClorRelief 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.