LETOMINT - clove tablet 
H&C 21 America Inc

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

active ingredient: clove

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

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

keep out of reach of the children

- 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


- 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

- 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
LETOMINT 
clove tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76255-2001
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLOVE (UNII: K48IKT5321) (CLOVE - UNII:K48IKT5321) CLOVE18 mg
Inactive Ingredients
Ingredient NameStrength
ALUMINUM SULFATE (UNII: 34S289N54E)  
GARLIC (UNII: V1V998DC17)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE (UNII: V5VD430YW9)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorwhite (ivory white) Scoreno score
ShapeOVAL (tablet) Size10mm
FlavorImprint Code 3;hp;x
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76255-2001-118 in 1 BOX
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/18/2011
Labeler - H&C 21 America Inc (968313267)
Registrant - H&C 21 America Inc (968313267)
Establishment
NameAddressID/FEIBusiness Operations
GM Manufacturing Inc102301749manufacture

Revised: 6/2011
Document Id: dd69ed67-5608-4dbd-9543-48734bef70f7
Set id: fe10b461-11a8-4d0b-9774-dcdbd8517953
Version: 1
Effective Time: 20110618
 
H&C 21 America Inc