EGOLAN

Manufacturer
Sanrace Biotechnology Co., Ltd.
Effective date
2020-08-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:24

Label at a glance#

ProductEGOLAN
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• To decrease bacteria on the skin that could cause disease. • Recommended for repeated use.

Dosage and administration

• Wet hands thoroughly with product and allow to dry without wiping. • For children under 6, use only under adult supervision. • Not recommended for infants.

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• To decrease bacteria on the skin that could cause disease.

• Recommended for repeated use.

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

STORAGE AND HANDLING SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75448-026-01EGOLAN500 mL in 1 BOTTLE, PLASTICGEL5001
75448-026-02EGOLAN2 in 1 BLISTER PACKGEL21
75448-026-03EGOLAN30 mL in 1 BOTTLE, PLASTICGEL301
75448-026-04EGOLAN30 mL in 1 BOTTLE, PLASTICGEL301
75448-026-05EGOLAN30 mL in 1 BOTTLE, PLASTICGEL301
75448-026-06EGOLAN30 mL in 1 BOTTLE, PLASTICGEL301
75448-026-07EGOLAN60 mL in 1 BOTTLE, PLASTICGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75448-026EGOLAN (ETHYL ALCOHOL) GEL [SANRACE BIOTECHNOLOGY CO., LTD.]1Legacy NDC, 7 package rows20200811_f75f7c24-1ebd-4255-95e8-1fb0298dbb69.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75448-02675448-026-03, 75448-026-04, 75448-026-05, 75448-026-06, 75448-026-07, 75448-026-02, 75448-026-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
30195380-b6d3-4168-a472-5bc9cfae3e1df75f7c24-1ebd-4255-95e8-1fb0298dbb692020-08-04WarningsExact identifier
spl id: 30195380-b6d3-4168-a472-5bc9cfae3e1d
spl set id: f75f7c24-1ebd-4255-95e8-1fb0298dbb69

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.