FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:16:29

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough Product in your plam to thoroughly spread on both hands and rubinto skin until dry. Children under 6 years of age should be supervised when using this product

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol75% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Uses Hand Sanitizer to held reduce bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire source when using For sxternal use only.

Do not use

OTC - DO NOT USE SECTION

  • do not use in or near the eyes

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes. In case of contact, rinseeyes thoroughly with water Stop use and ask doctor if irritation or rash appears andlasts. Keep out of reach for children. If swallowed, get medical help or contact a PoisonControl Center right away

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or rash appedears anclasts.

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 Product in your plam to thoroughly spread on both hands and rubinto skin until dry.
    Children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, carbomer, aloe barbadensis leaf extract,taraxacum officinale( dandelion )rhizome/root extract, lonicera japonica flowerextract, triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3311

22

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75209-008-012022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-022022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-032022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-042022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-052022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-062022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-072022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-082022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-092022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-102022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-112022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-122022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc
75209-008-132022-01-28C16284748780-1d6a99b39-db2f-a426-e053-dadaa90af4c2a380dd11-4f1a-2979-e053-2a95a90a83dc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75209-008-01Instant Hand Sanitizer50 mL in 1 BOTTLEGEL502
75209-008-02Instant Hand Sanitizer60 mL in 1 BOTTLEGEL602
75209-008-03Instant Hand Sanitizer120 mL in 1 BOTTLEGEL1202
75209-008-04Instant Hand Sanitizer200 mL in 1 BOTTLEGEL2002
75209-008-05Instant Hand Sanitizer500 mL in 1 BOTTLEGEL5002
75209-008-06Instant Hand Sanitizer30 mL in 1 BOTTLEGEL302
75209-008-07Instant Hand Sanitizer1000 mL in 1 BOTTLEGEL10002
75209-008-08Instant Hand Sanitizer2.8 mL in 1 BOTTLEGEL2.82
75209-008-09Instant Hand Sanitizer236 mL in 1 BOTTLEGEL2362
75209-008-10Instant Hand Sanitizer300 mL in 1 BOTTLEGEL3002
75209-008-11Instant Hand Sanitizer100 mL in 1 BOTTLEGEL1002
75209-008-12Instant Hand Sanitizer3800 mL in 1 BOTTLEGEL38002
75209-008-13Instant Hand Sanitizer4000 mL in 1 BOTTLEGEL40002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75209-008INSTANT HAND SANITIZER (ALCOHOL) GEL [GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.]2Legacy NDC, 13 package rows20200609_a380dd11-4f1a-2979-e053-2a95a90a83dc.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
75209-00875209-008-01, 75209-008-02, 75209-008-03, 75209-008-04, 75209-008-05, 75209-008-06, 75209-008-07, 75209-008-08, 75209-008-09, 75209-008-10, 75209-008-11, 75209-008-12, 75209-008-13

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
TARAXACUM OFFICINALE ROOT9DE5YCO0RUIACT
CARBOMER 934Z135WT9208IACT
ALOEV5VD430YW9IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT

Source Document#

Source XML · Source PDF

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
a79f29a6-927d-1541-e053-2995a90a28bea380dd11-4f1a-2979-e053-2a95a90a83dc2020-06-08WarningsExact identifier
spl id: a79f29a6-927d-1541-e053-2995a90a28be
spl set id: a380dd11-4f1a-2979-e053-2a95a90a83dc

Reported adverse events (FAERS/openFDA)#

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