EGOLAN- ethyl alcohol gel

EGOLAN by

Drug Labeling and Warnings

EGOLAN by is a Otc medication manufactured, distributed, or labeled by Sanrace Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

INDICATIONS & USAGE

Use: Hand sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from fire or flame.

For external use only. do not inhale or ingest.

Do not use in, or near the eyes. In case of contact with eyes, rinse thoroughly with water.

Avoid contact with broken skin

Stop use and ask a doctor if irritation or rash develops and persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

For children under 6, use only under adult supervision

Not recommended for infants

Other Information

Store below 110°F (43°C)

May discolor certain fabrics or surfaces

Inactive ingredients

Water,Glycerin,Propylene Glycol,Triethanolamine,Carbomer,Aloe Vera Gel

SPL UNCLASSIFIED SECTION

ANTIBACTERIAL

KILLS 99.9% GERMS

Manufacturer:

Sanrace Biotechnology Co., Ltd

Manufacturer Address:268 Yanzhou Road,

Lanxi Development Zone,Zhejiang Province.

Made In China.

Packaging

INGREDIENTS AND APPEARANCE

EGOLAN 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75448-023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75448-023-03	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - Sanrace Biotechnology Co., Ltd. (543000938)

Establishment
Name	Address	ID/FEI	Business Operations
Sanrace Biotechnology Co., Ltd.		543000938	manufacture(75448-023)