FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Zhongshan Chuanlin Biotechnology Co., Ltd.
Effective date
2020-04-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:08:31

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer helps reduce bacteria on the skin.

Dosage and administration

Put enough product in your palm to spread your hands thoroughly and rub into the skin until dry. Children under 6 should be supervised when using this product.

Storage and handling

Store at：106°F(41°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

75% ethanol

purpose

OTC - PURPOSE SECTION

antibacterial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer helps reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable,away from fire or open flames, for external use only.

When using this product

OTC - WHEN USING SECTION

do not use it in or near your eyes.In case of contact, rinse eyes thoroughly with water.Discontinue use and ask your doctor if there is and continued irritation or rash.Keep out of reach of children.If swallowed,consult a doctor immediately or contact a poison control center.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to spread your hands

thoroughly and rub into the skin until dry.

Children under 6 should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store at：106°F(41°C)

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized water, carbomer,

triethanolamine,glycerol,propylene glycol

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 ml label30 ml label60 ml label60 ml label90 ml label90 ml label300 ml label300 ml label500 ml label500 ml label800 ml label800 ml label1000 ml label1000 ml label2000 ml label2000 ml label5000 ml label5000 ml label

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
75142-001-012022-01-28C16284748780-1d6a99b39-8a6b-a426-e053-dadaa90af4c2Hand Sanitizer
75142-001-022022-01-28C16284748780-1d6a99b39-8a6b-a426-e053-dadaa90af4c2Hand Sanitizer
75142-001-032022-01-28C16284748780-1d6a99b39-8a6b-a426-e053-dadaa90af4c2Hand Sanitizer
75142-001-042022-01-28C16284748780-1d6a99b39-8a6b-a426-e053-dadaa90af4c2Hand Sanitizer
75142-001-052022-01-28C16284748780-1d6a99b39-8a6b-a426-e053-dadaa90af4c2Hand Sanitizer
75142-001-062022-01-28C16284748780-1d6a99b39-8a6b-a426-e053-dadaa90af4c2Hand Sanitizer
75142-001-072022-01-28C16284748780-1d6a99b39-8a6b-a426-e053-dadaa90af4c2Hand Sanitizer
75142-001-082022-01-28C16284748780-1d6a99b39-8a6b-a426-e053-dadaa90af4c2Hand Sanitizer
75142-001-092022-01-28C16284748780-1d6a99b39-8a6b-a426-e053-dadaa90af4c2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75142-001-01Hand Sanitizer30 mL in 1 BOTTLEGEL301
75142-001-02Hand Sanitizer60 mL in 1 BOTTLEGEL601
75142-001-03Hand Sanitizer90 mL in 1 BOTTLEGEL901
75142-001-04Hand Sanitizer300 mL in 1 BOTTLEGEL3001
75142-001-05Hand Sanitizer500 mL in 1 BOTTLEGEL5001
75142-001-06Hand Sanitizer800 mL in 1 BOTTLEGEL8001
75142-001-07Hand Sanitizer1000 mL in 1 BOTTLEGEL10001
75142-001-08Hand Sanitizer2000 mL in 1 BOTTLEGEL20001
75142-001-09Hand Sanitizer5000 mL in 1 BOTTLEGEL50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75142-001HAND SANITIZER GEL [ZHONGSHAN CHUANLIN BIOTECHNOLOGY CO., LTD.]1Legacy NDC, 9 package rows20200429_a3a3d036-0a6f-b346-e053-2995a90aa102.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75142-00175142-001-01, 75142-001-02, 75142-001-03, 75142-001-04, 75142-001-05, 75142-001-06, 75142-001-07, 75142-001-08, 75142-001-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT

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
a3a3dc48-9dda-9869-e053-2a95a90a7092a3a3d036-0a6f-b346-e053-2995a90aa1022020-04-19WarningsExact identifier
spl id: a3a3dc48-9dda-9869-e053-2a95a90a7092
spl set id: a3a3d036-0a6f-b346-e053-2995a90aa102

Reported adverse events (FAERS/openFDA)#

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