FDA.reportPublic FDA data

5Seconds Advanced Hand Sanitizer

Manufacturer
AVS Energy Inc | Zhejiang Shenying Technology Co., Ltd. Jiaojiang Branch
Effective date
2020-10-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:24

Label at a glance#

Product5Seconds Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Place enough products in your palm to thoroughly cover your hands Rub hands together briskly until dry No rinsing required No towels needed

Storage and handling

Do not store above 110F (43C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough products in your palm to thoroughly cover your hands

Rub hands together briskly until dry

No rinsing required

No towels needed

Other information

STORAGE AND HANDLING SECTION

Do not store above 110F (43C)

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Glycerol, Vitamin E,  Aloe Vera Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77871-004-012022-01-28C16284748780-1d6a99b39-e4b9-a426-e053-dadaa90af4c2b600cbd1-b0e0-4689-8268-1261cd854dae
77871-004-022022-01-28C16284748780-1d6a99b39-e4b9-a426-e053-dadaa90af4c2b600cbd1-b0e0-4689-8268-1261cd854dae
77871-004-032022-01-28C16284748780-1d6a99b39-e4b9-a426-e053-dadaa90af4c2b600cbd1-b0e0-4689-8268-1261cd854dae
77871-004-042022-01-28C16284748780-1d6a99b39-e4b9-a426-e053-dadaa90af4c2b600cbd1-b0e0-4689-8268-1261cd854dae
77871-004-052022-01-28C16284748780-1d6a99b39-e4b9-a426-e053-dadaa90af4c2b600cbd1-b0e0-4689-8268-1261cd854dae
77871-004-062022-01-28C16284748780-1d6a99b39-e4b9-a426-e053-dadaa90af4c2b600cbd1-b0e0-4689-8268-1261cd854dae
77871-004-072022-01-28C16284748780-1d6a99b39-e4b9-a426-e053-dadaa90af4c2b600cbd1-b0e0-4689-8268-1261cd854dae

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77871-004-015Seconds Advanced Hand Sanitizer60 mL in 1 BOTTLEGEL601
77871-004-025Seconds Advanced Hand Sanitizer100 mL in 1 BOTTLEGEL1001
77871-004-035Seconds Advanced Hand Sanitizer237 mL in 1 BOTTLEGEL2371
77871-004-045Seconds Advanced Hand Sanitizer500 mL in 1 BOTTLEGEL5001
77871-004-055Seconds Advanced Hand Sanitizer1000 mL in 1 BOTTLEGEL10001
77871-004-065Seconds Advanced Hand Sanitizer2000 mL in 1 BOTTLEGEL20001
77871-004-075Seconds Advanced Hand Sanitizer3785 mL in 1 BOTTLEGEL37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77871-0045SECONDS ADVANCED HAND SANITIZER (ALCOHOL) GEL [AVS ENERGY INC]1Legacy NDC, 7 package rows20201011_b600cbd1-b0e0-4689-8268-1261cd854dae.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77871-00477871-004-01, 77871-004-02, 77871-004-03, 77871-004-04, 77871-004-05, 77871-004-06, 77871-004-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCEROL FORMAL3L7GR2604EIACT
ALOE VERA WHOLEKIZ4X2EHYXIACT
CARBOMER 9404Q93RCW27EIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB

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
b15cf814-38e6-de69-e053-2995a90ad424b600cbd1-b0e0-4689-8268-1261cd854dae2020-10-10WarningsExact identifier
spl id: b15cf814-38e6-de69-e053-2995a90ad424
spl set id: b600cbd1-b0e0-4689-8268-1261cd854dae

Reported adverse events (FAERS/openFDA)#

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