DRx Choice Fiber Therapy

DRx Choice Fiber Therapy is an FDA-registered drug product whose active ingredient is METHYLCELLULOSE. It is labelled by RARITAN PHARMACEUTICALS INC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 68163-517, application M007, label effective 20260908. It is one of 5 FDA drug label records sharing the active ingredient METHYLCELLULOSE. 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 METHYLCELLULOSE 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 a bowel movement in 12-72 hours

Directions • MIX THIS PRODUCT (CHILD OR ADULT DOSE) WITH AT LEAST 8 OUNCES (A FULL GLASS) OF WATER OR OTHER FLUID. TAKING THIS PRODUCT WITHOUT ENOUGH LIQUID MAY CAUSE CHOKING. SEE CHOKING WARNING • use product at the first sign of constipation or irregularity • put one dose in a full glass of cold water • stir briskly and drink promptly • drinking another glass of water is helpful Age Dose adults & children 12 years of age and over start with 1 rounded tablespoon . Increase as needed, 1 rounded tablespoon at a time, up to 3 times per day. children 6 - 11 years of age start with 2 level teaspoons . Increase as needed, 2 level teaspoons at a time, up to 3 times per day. children under 6 years of age consult a physician

Warnings Choking: taking this product without adequate fluid may cause it to swell and block your throat or esophagus and may cause choking. Do not take this product if you have difficulty in swallowing. If you experience chest pain, vomiting, or difficulty in swallowing or breathing after taking this product, seek immediate medical attention. Ask a doctor before use if you have ▪ a sudden change in bowel habits that persists for two weeks ▪ abdominal pain, nausea or vomiting Stop use and ask a doctor if ▪ constipation lasts more than 7 days ▪ you have rectal bleeding These could be signs of a serious condition. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

FDA lists 5 drug label records with METHYLCELLULOSE 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 DRx Choice Fiber Therapy used for?
Uses ▪ relieves occasional constipation (irregularity) ▪ generally produces a bowel movement in 12-72 hours

Who makes DRx Choice Fiber Therapy?
RARITAN PHARMACEUTICALS INC is the labeler of record for DRx Choice Fiber Therapy. 5 FDA label records share the active ingredient METHYLCELLULOSE, 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 DRx Choice Fiber Therapy 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 DRx Choice Fiber Therapy 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 METHYLCELLULOSE?
Yes. 5 FDA drug label records list METHYLCELLULOSE 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 DRx Choice Fiber Therapy 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.