Mantra

Mantra is an FDA-registered drug product whose active ingredient is MANTRA SLEEP AID WILD CHERRY. It is labelled by MOREMED INC. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 85410-040, application M010, label effective 20260727. 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 MANTRA SLEEP AID WILD CHERRY are most often described in connection with: helps reduce, difficulty falling. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Helps to reduce difficulty falling asleep

Directions Take only one dose (1 Pouch) per day (24 hours) Adults and children 12 years and over:1 Pouch at bedtime if needed, or as directed by a doctor

Warnings Do not use for children under 12 years of age with any other products containing diphenhydramine, even one used on skin Ask a doctor before use if you have a breathing problem such as emphysema or chronic bronchitis, glaucoma or difficulty in urinating due to enlargement of the prostate gland Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers, When using this product avoid alcoholic beverages Stop use and ask a doctor if Sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of a serious underlying medical illness. If Pregnant or breastfeeding ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a poison control Centre right away.

What is Mantra used for?
Helps to reduce difficulty falling asleep

Who makes Mantra?
MOREMED INC. is the labeler of record for Mantra.

What form does Mantra 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 Mantra 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 Mantra 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.