ELAS GEL- troxerutin, ginkgo lotion

Elas gel by

Drug Labeling and Warnings

Elas gel by is a Otc medication manufactured, distributed, or labeled by Cho-A Pharm.Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Troxerutin (1500mg)

Ginkgo Leaf Extract (70mg)

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.

WARNINGS

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

INGREDIENTS AND APPEARANCE

ELAS GEL 
troxerutin, ginkgo lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58354-116
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GINKGO (UNII: 19FUJ2C58T) (GINKGO - UNII:19FUJ2C58T)	GINKGO	70 mg  in 50 g
TROXERUTIN (UNII: 7Y4N11PXO8) (TROXERUTIN - UNII:7Y4N11PXO8)	TROXERUTIN	1500 mg  in 50 g

Inactive Ingredients
Ingredient Name	Strength
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)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58354-116-02	1 in 1 PACKAGE	03/23/2019
1	NDC: 58354-116-01	50 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/23/2019

Labeler - Cho-A Pharm.Co.,Ltd. (688056831)

Registrant - Cho-A Pharm.Co.,Ltd. (688056831)

Establishment
Name	Address	ID/FEI	Business Operations
Cho-A Pharm.Co.,Ltd.		688056831	manufacture(58354-116)