Eversoft Foaming Hand Sanitizer

Manufacturer
Teh Tung Corporation
Effective date
2020-10-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:43

Label at a glance#

ProductEversoft Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Apply liberally to the hands and gently rub until dry.

Storage and handling

• Store above 0°C (32°F)

Label contents#

Full prescribing information#

Active Ingredient 

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol, 73%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

• Hand sanitizing to help reduce bacteria on the skin • Recommended for repeated use

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally to the hands and gently rub until dry.

Other Information

STORAGE AND HANDLING SECTION

• Store above 0°C (32°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Dimethicone, Isopropyl Alcohol

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame.

For external use only.

When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

SPL UNCLASSIFIED SECTION

Foaming Hand Sanitizer - Alcohol Form

*Patented formula effectively eliminates 99.99% of tested germs, bacteria and viruses in as little as 15 seconds; long-term protection for up to 12 hrs.

Distributed by:

Draco Hygienic Products Inc.

716 S. Bon View Ave, Ontario, CA 91761

www.draco.com

Emergency: Chemtel 800-2553924

WARNING: FLAMMABLE LIQUID AND VAPOR.

CAUSES SERIOUS EYE IRRITATION. HARMFUL IF SWALLOWED.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2462455ethanol 73 % Topical FoamPSN1
2462455ethanol 0.73 ML/ML Topical FoamSCD1
2462455ethanol 73 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78168-003-552022-01-28C16284748780-1d6a99b39-7e3a-a426-e053-dadaa90af4c2eversoft Foaming Hand Sanitizer
78168-003-562022-01-28C16284748780-1d6a99b39-7e3a-a426-e053-dadaa90af4c2eversoft Foaming Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78168-003-55Eversoft Foaming Hand Sanitizer1000 mL in 1 BOTTLELIQUID10001
78168-003-56Eversoft Foaming Hand Sanitizer3785 mL in 1 BOTTLELIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78168-003EVERSOFT FOAMING HAND SANITIZER (ETHYL ALCOHOL) LIQUID [TEH TUNG CORPORATION]1Legacy NDC, 2 package rows20201101_e3ce0695-bb85-46fb-b370-2023207752ce.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78168-00378168-003-55, 78168-003-56

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
b1d484f9-8809-46ad-8090-0099edc7d3c5e3ce0695-bb85-46fb-b370-2023207752ce2020-10-21WarningsExact identifier
spl id: b1d484f9-8809-46ad-8090-0099edc7d3c5
spl set id: e3ce0695-bb85-46fb-b370-2023207752ce

Reported adverse events (FAERS/openFDA)#

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