EGOLAN- ethyl alcohol gel 
Sanrace Biotechnology Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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EGOLAN® HAND SANITIZER

Drug Facts

Active ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

■ To decrease bacteria on the skin that could cause disease. ■ When water, soap, and towel are not available. ■ Recommended for repeated use.

Warnings

For external use only: hands.

Flammable. Keep away from fire or flame.

When using this product ■ Keep out of eyes, ears, or mouth. ■ In case of eye contact, flush eyes thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale or ingest.

Stop use and ask a doctor if ■ redness or irritation develop ■ condition persists for more than 72 hours

Keep out of reach of children. ■ Children should be supervised by an adult when using this product. ■ If swallowed, get medical help or contact a Poison Control Center right away.

Directions ■ Wet hands thoroughly with product and allow to dry without wiping. ■ No rinsing required. ■ For children under 6, use only under adult supervision. ■ Not recommended for infants.

Other information ■ Store below 105°F (40°C). ■ May discolor certain fabrics. ■ Harmful to wood finishes & plastics.

Inactive ingredients: Water (Aqua), Triethanolamine, Carbomer, Aloe Barbadensis (Aloe Vera) Gel, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E).

KILLS 99.9% OF GERMS

ADVANCED MOISTURIZING FORMULA WITH ALOE AND VITAMIN E

Manufacturer: Sanrace Biotechnology Co., Ltd.

Address: 268 Yanzhou Road, Lanxi Economic Development zone, Zhejiang Province.

Made in China

Packaging

IMAGE1IMAGE2IMAGE3

EGOLAN 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75448-027
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75448-027-2360 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/01/2020
2NDC:75448-027-222 in 1 BLISTER PACK08/01/2020
2NDC:75448-027-2360 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:75448-027-21237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/01/2020
Labeler - Sanrace Biotechnology Co., Ltd. (543000938)
Establishment
NameAddressID/FEIBusiness Operations
Sanrace Biotechnology Co., Ltd.543000938manufacture(75448-027)

Revised: 8/2020
Document Id: c2e80852-3bb9-41c7-a83b-e341ba01c8f7
Set id: fe16d57b-469e-4158-b719-80fd18d9d858
Version: 1
Effective Time: 20200806
 
Sanrace Biotechnology Co., Ltd.