ELAS GEL- troxerutin, ginkgo lotion 
Cho-A Pharm.Co.,Ltd.

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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Elas gel

Active Ingredients

Troxerutin (3000mg)

Ginkgo Leaf Extract (140mg)

Purpose

Topical Analgesic

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center(1-800-222-1222) right away.

Uses

For the temporarily relieves the symptoms of pain, swelling, bruising.

For external use only
Use only the recommended dosage
Do not use on mucous membrane, damaged or broken skin
When using this product
 Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and ask doctor if rash or irritation on skin develops and lasts.
If pregnant or breast-feeding, ask a health professional before use.

Store at room temperature

Directions

Apply the adequate amount to affected skin 2-4 times in a day and massage lightly.

Inactive Ingredients

Carbopol 940, Methylparaben, Propylparaben, Sodium Hydroxide, Disodium Edetate Hydrate, Isopropanol, Purified Water

Elas gel

elas gel label

ELAS GEL 
troxerutin, ginkgo lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58354-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GINKGO (UNII: 19FUJ2C58T) (GINKGO - UNII:19FUJ2C58T) GINKGO140 mg  in 100 g
TROXERUTIN (UNII: 7Y4N11PXO8) (TROXERUTIN - UNII:7Y4N11PXO8) TROXERUTIN3000 mg  in 100 g
Inactive Ingredients
Ingredient NameStrength
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58354-102-021 in 1 PACKAGE02/28/2017
1NDC:58354-102-01100 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/28/201705/18/2023
Labeler - Cho-A Pharm.Co.,Ltd. (688056831)
Registrant - Cho-A Pharm.Co.,Ltd. (688056831)
Establishment
NameAddressID/FEIBusiness Operations
Cho-A Pharm.Co.,Ltd.688056831manufacture(58354-102)

Revised: 5/2023
 
Cho-A Pharm.Co.,Ltd.