Letomint

Manufacturer
H&C 21 America Inc | GM Manufacturing Inc
Effective date
2011-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:28:24

Label at a glance#

ProductLetomint
Active ingredientCLOVE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredient: clove

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

- 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 SECTION

- 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 SECTION

- 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CLOVE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76255-2001-12019-10-29C16284748780-1960f7f55-d100-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76255-2001-1Letomint18 in 1 BOXTABLET181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76255-2001LETOMINT (CLOVE) TABLET [H&C 21 AMERICA INC]1Legacy NDC, 1 package rows20110623_fe10b461-11a8-4d0b-9774-dcdbd8517953.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CLOVEACTIVE INGREDIENTK48IKT53211
CLOVEACTIVE MOIETYK48IKT53211
ALOEINACTIVE INGREDIENTV5VD430YW91
ALPHA-TOCOPHEROL ACETATEINACTIVE INGREDIENT9E8X80D2L01
ALUMINUM SULFATEINACTIVE INGREDIENT34S289N54E1
GARLICINACTIVE INGREDIENTV1V998DC171
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1A1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76255-200176255-2001-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALUMINUM SULFATEALUMINUM SULFATE34S289N54ECREAM / TOPICAL14 mgExact identifier — unii candidate
ALPHA-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
3 equally ranked IID candidates
ALPHA-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0TABLET / ORAL0.5 mgExact identifier — unii candidate
3 equally ranked IID candidates
ALPHA-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0CAPSULE / ORAL2 mgExact identifier — unii candidate
3 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
dd69ed67-5608-4dbd-9543-48734bef70f7fe10b461-11a8-4d0b-9774-dcdbd85179532011-06-18WarningsExact identifier
spl id: dd69ed67-5608-4dbd-9543-48734bef70f7
spl set id: fe10b461-11a8-4d0b-9774-dcdbd8517953

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.