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.

Recommended for repeated use.

Warnings

For external use only-hands. Flammable.

Keep away from heat and flame. When using this product Keep out of eyes. In case of contact with eyes, flush thoroughly with water.  Avoid contact with broken skin.  Do not inhale or ingest. Stop use and ask a doctor if skin irritation develops.

Keep out of reach of children. In case of accidental ingestion, seek professional assistance 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

Do not store above 105°F.  May discolor some fabrics  Harmful to wood finishes and plastics.

Inactive Ingredients

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Aloe Barbadensis Leaf Extract,Triethanolamine, Disodium EDTA, Tocophery Acetate (Vitamin E), Fragrance.

SPL UNCLASSIFIED SECTION

KILLS 99.9% OF GERMS

ALOE VERA SOOTHING GEL

70% ALCOHOL

STAY SAFE

Keep your hands clean on the go with Alchemy Living 2 Pc Hand Sanitizer set. Helps reduce bacteria on

the skin while leaving hands feeling smooth.

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: 75448-026
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)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75448-026-03	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2020
2	NDC: 75448-026-04	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2020
3	NDC: 75448-026-05	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2020
4	NDC: 75448-026-06	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2020
5	NDC: 75448-026-07	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/01/2020
6	NDC: 75448-026-02	2 in 1 BLISTER PACK	08/01/2020
6	NDC: 75448-026-07	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7	NDC: 75448-026-01	500 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(75448-026)