Letomint
FDA Label NDC 76255-2001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by H&c 21 America Inc for the product Letomint (NDC 76255-2001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active ingredient: clove

Inactive Ingredient

Inactive ingredient:  aluminium sulfate, garlic, polyethylens glycols, vitamin E, aloe, water, sepia esculenta, galla rhois

Otc - Purpose

Improvement of vaginal discharge, leukorrhea, vperiod pain and menstrual irregularity

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

- if you put this into your vaginas deeply, it will show its effectsas- it melts and soaked into your skin by itself after 30~40 minutes- please make sure to check sediments by having a sitz batn- your wombs will get back to healthy of twenties if you continue to use one pill per 2~3days

Warnings

- please do not use it during the period or if you are pregnant- store avoid direct sunlight, high temperatures, and humidity- keep in a cool and dry place

Dosage & Administration

- women that the lower abdoment or the hands and feet are cold- women who have period pain and menstrual irregularity or have a light or heavy flow during your period- women that have serious vaginal discharge- women who try to prevent urinary incontinence- women who feel that their vaginal muscle is relaxed after delivery

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