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 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.

DOSAGE & ADMINISTRATION

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.

STORAGE AND HANDLING

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

INACTIVE INGREDIENT

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

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

EGOLAN 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75448-027
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75448-027-23	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2020
2	NDC: 75448-027-22	2 in 1 BLISTER PACK	08/01/2020
2	NDC: 75448-027-23	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 75448-027-21	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/01/2020

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

Establishment
Name	Address	ID/FEI	Business Operations
Sanrace Biotechnology Co., Ltd.		543000938	manufacture(75448-027)