Hand Sanitizer

Manufacturer
GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.
Effective date
2020-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:49

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

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 above105°F. May discolor some fabrics. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For Hand Sanitizing

Warnings

WARNINGS SECTION

For external use only-hands.
Flammable. Keep away from heat and flame.

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.

Do not inhale or ingest.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops.

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

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 above105°F.
May discolor some fabrics.
Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30305353606030 230 2

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
75209-009-012022-01-28C16284748780-1d6a99b39-a884-a426-e053-dadaa90af4c2Hand Sanitizer
75209-009-022022-01-28C16284748780-1d6a99b39-a884-a426-e053-dadaa90af4c2Hand Sanitizer
75209-009-032022-01-28C16284748780-1d6a99b39-a884-a426-e053-dadaa90af4c2Hand Sanitizer
75209-009-042022-01-28C16284748780-1d6a99b39-a884-a426-e053-dadaa90af4c2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75209-009-01Hand Sanitizer30 mL in 1 BOTTLEGEL301
75209-009-02Hand Sanitizer30 mL in 1 BOTTLEGEL301
75209-009-03Hand Sanitizer53 mL in 1 BOTTLEGEL531
75209-009-04Hand Sanitizer60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75209-009HAND SANITIZER GEL [GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.]1Legacy NDC, 4 package rows20200603_a71810ae-0da6-dd8e-e053-2995a90a7cf4.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75209-00975209-009-04, 75209-009-02, 75209-009-03, 75209-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
a71810ae-0da4-dd8e-e053-2995a90a7cf4a71810ae-0da6-dd8e-e053-2995a90a7cf42020-06-02WarningsExact identifier
spl id: a71810ae-0da4-dd8e-e053-2995a90a7cf4
spl set id: a71810ae-0da6-dd8e-e053-2995a90a7cf4

Reported adverse events (FAERS/openFDA)#

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