CANTHARIS 30C

CANTHARIS 30C is an FDA-registered drug product whose active ingredient is LYTTA VESICATORIA. It is labelled by Natural Creations, Inc. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 43406-0461, label effective 20221219. It is one of 11 FDA drug label records sharing the active ingredient LYTTA VESICATORIA. 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 LYTTA VESICATORIA are most often described in connection with: temporarily relieves, constant desire. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

USES : Temporarily relieves constant desire to urinate.**

DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care provider.

WARNINGS: Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.

FDA lists 11 drug label records with LYTTA VESICATORIA 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 CANTHARIS 30C used for?
USES : Temporarily relieves constant desire to urinate.**

Who makes CANTHARIS 30C?
Natural Creations, Inc. is the labeler of record for CANTHARIS 30C. 11 FDA label records share the active ingredient LYTTA VESICATORIA, 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 CANTHARIS 30C 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 CANTHARIS 30C 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 LYTTA VESICATORIA?
Yes. 11 FDA drug label records list LYTTA VESICATORIA 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 CANTHARIS 30C 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.