JILGYUNGYI  - allantoin tablet 
HA U DONG CHUN

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.

----------

Drug Facts

allantoin


sodium chloride, collagen, glucose, magnesium stearate, aloe extract, opuntia ficus-indica extract, mentha aryensis extract, centella asiatica extract, sophora flavescens aiton extract, angelica acutiloba extract


- relives the following symtoms
  yeast infection, vaginal itching and irritaiton, vaginal dryness and odor, menstrual cramps, urinary incontinence, vaginal thghtness


keep out of reach of the children


This product is to be used in the vagina. Use it at bedtime, or during the day without dynamic activities. Insert the pills into your vagina with first two knuckles of your finger. During the 20 to 30 minutes the pills are melted and they are effective in improving vaginal health

• Do not use during pregnant, breast-feeding, or menstrual cycle
• Keep this product out of reach of children under 3 years old

for vaginal use only


package insert
JILGYUNGYI  
allantoin tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55618-1001
Route of AdministrationVAGINAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.2 
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
COLLAGENASE CLOSTRIDIUM HISTOLYTICUM (UNII: 9X7O8V25IT)  
DEXTROSE (UNII: IY9XDZ35W2)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
ALOE (UNII: V5VD430YW9)  
OPUNTIA FICUS-INDICA (UNII: 23Z87HTQ6P)  
MENTHA ARVENSIS FLOWER OIL (UNII: Q129Z1W6Y2)  
CENTELLA ASIATICA (UNII: 7M867G6T1U)  
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
ANGELICA ACUTILOBA ROOT OIL (UNII: 96L0Z12X98)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeOVAL (tablet) Size12mm
FlavorImprint Code 3;hp;x
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55618-1001-120 in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/11/2013
Labeler - HA U DONG CHUN (688479464)
Registrant - HA U DONG CHUN (688479464)
Establishment
NameAddressID/FEIBusiness Operations
HA U DONG CHUN688479464manufacture(55618-1001)

Revised: 6/2013
Document Id: 62bbe3ca-4f5c-4dab-a559-00cdbd1c0365
Set id: 0579fcc7-e0c8-4958-8ab4-1ac8e8f7d88f
Version: 4
Effective Time: 20130611
 
HA U DONG CHUN