OneLAX Saline Laxative

OneLAX Saline Laxative is an FDA-registered drug product whose active ingredient is MAGNESIUM CITRATE. It is labelled by AKRON PHARMA INC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 71399-0051, application M007, label effective 20260901. It is one of 9 FDA drug label records sharing the active ingredient MAGNESIUM CITRATE. 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 MAGNESIUM CITRATE are most often described in connection with: relieves occasional, constipation irregularity, generally produces, bowel movement. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses relieves occasional constipation (irregularity) generally produces bowel movement in 1/2 to 6 hours

Directions drink a full glass (8 ounces) of liquid with each dose. may be taken as a single daily dose or in divided doses. adults and children 12 years of age and over 1/2 bottle to 1 bottle (10 fl oz) children 6 to 11 years of age 1/3 bottle to 1/2 bottle children under 6 years of age consult a doctor

Warnings Do not use laxative products for longer than 1 week unless directed by a doctor. Ask a doctor before use if you have kidney disease a magnesium restricted diet a sodium restricted diet stomach pain, nausea or vomiting noticed a sudden change in bowel habits that lasts more than 1 week Ask a doctor or pharmacist before use if you are presently taking a prescription drug. When using this product do not exceed the maximum recommended daily dosage in a 24 hour period. Stop use and ask a doctor if you have rectal bleeding or no bowel movement after use. These could 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 (1-800-222-1222) right away.

FDA lists 9 drug label records with MAGNESIUM CITRATE 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 OneLAX Saline Laxative used for?
Uses relieves occasional constipation (irregularity) generally produces bowel movement in 1/2 to 6 hours

Who makes OneLAX Saline Laxative?
AKRON PHARMA INC is the labeler of record for OneLAX Saline Laxative. 9 FDA label records share the active ingredient MAGNESIUM CITRATE, 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 OneLAX Saline Laxative 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 OneLAX Saline Laxative 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 MAGNESIUM CITRATE?
Yes. 9 FDA drug label records list MAGNESIUM CITRATE 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 OneLAX Saline Laxative 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.