Hand Sanitizer Antibacterial

Manufacturer
Ningbo Yinzhou Lvguang International Trade Co.,Ltd | NINGHAI WEIYI DAYLY NECESSITIES FACTORY
Effective date
2020-05-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:00

Label at a glance#

ProductHand Sanitizer Antibacterial
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

for handwashing to decrease bacteria on the skin recommended for repeated use

Dosage and administration

Directions wet hands thoughly with product briskly rub hands together until dry supervise children 6 years of age in the use of this product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62.0% Antimicrobial

Purpose

OTC - PURPOSE SECTION

Purpose - Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from heat and flame.

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes, in case of contact, rinse eyes throughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persist for more then 72 hours

Keep out of reach children

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

Directions

  • wet hands thoughly with product
  • briskly rub hands together until dry
  • supervise children 6 years of age in the use of this product

Other Information

OTHER SAFETY INFORMATION

Other Information

  • store at room temperature
  • may discolor certain fabrics

Questions/Comments

OTC - QUESTIONS SECTION

​Questions/Comments?

sales03@nb-greenlight.com

DISTRIBUTED BY:
NINGBO YINZHOU GREENLIGHT INTERNATIONAL CO.,LTD

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients

water,glycerin,carbomer, fragrance, triethanolamine, propylene glycol, aloe barbadensis leaf juice, tocopheryl acetate, fd&blue no.1, fd&yellow no.5

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

77125-002-01 NDC 236 ml

236 ml hand sanitizer label236 ml hand sanitizer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77125-002-012021-07-23C16284748780-1c7ccaba7-1e99-fd44-e053-dadaa90aa01bHand Sanitizer Antibacterial

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77125-002-01Hand Sanitizer Antibacterial236 mL in 1 BOTTLE, PLASTICGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77125-002HAND SANITIZER ANTIBACTERIAL (ETHYL ALCOHOL) GEL [NINGBO YINZHOU LVGUANG INTERNATIONAL TRADE CO.,LTD]1Legacy NDC, 1 package rows20200507_a50235a7-700b-deaa-e053-2995a90a35bf.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77125-00277125-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
a5023e84-c80c-229b-e053-2995a90afc5ca50235a7-700b-deaa-e053-2995a90a35bf2020-05-06WarningsExact identifier
spl id: a5023e84-c80c-229b-e053-2995a90afc5c
spl set id: a50235a7-700b-deaa-e053-2995a90a35bf

Reported adverse events (FAERS/openFDA)#

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