FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Shantou Wanli Biotechnology Co.,Ltd.
Effective date
2020-06-02
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:15:44

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

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

PROPYL ALCOHOL 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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 on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

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

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

16160505060607070808090910101111010102020303

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN5
1305100ethanol 0.75 ML/ML Topical GelSCD5
1305100ethanol 75 % Topical GelSY5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74928-002-012022-01-28C16284748780-1d6a99b39-8de6-a426-e053-dadaa90af4c2a305d255-9668-0854-e053-2995a90ac5f9
74928-002-022022-01-28C16284748780-1d6a99b39-8de6-a426-e053-dadaa90af4c2a305d255-9668-0854-e053-2995a90ac5f9
74928-002-032022-01-28C16284748780-1d6a99b39-8de6-a426-e053-dadaa90af4c2a305d255-9668-0854-e053-2995a90ac5f9
74928-002-042022-01-28C16284748780-1d6a99b39-8de6-a426-e053-dadaa90af4c2a305d255-9668-0854-e053-2995a90ac5f9
74928-002-052022-01-28C16284748780-1d6a99b39-8de6-a426-e053-dadaa90af4c2a305d255-9668-0854-e053-2995a90ac5f9
74928-002-062022-01-28C16284748780-1d6a99b39-8de6-a426-e053-dadaa90af4c2a305d255-9668-0854-e053-2995a90ac5f9
74928-002-072022-01-28C16284748780-1d6a99b39-8de6-a426-e053-dadaa90af4c2a305d255-9668-0854-e053-2995a90ac5f9
74928-002-082022-01-28C16284748780-1d6a99b39-8de6-a426-e053-dadaa90af4c2a305d255-9668-0854-e053-2995a90ac5f9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74928-002-01HAND SANITIZER30 mL in 1 BOTTLEGEL305
74928-002-02HAND SANITIZER60 mL in 1 BOTTLEGEL605
74928-002-03HAND SANITIZER100 mL in 1 BOTTLEGEL1005
74928-002-04HAND SANITIZER200 mL in 1 BOTTLEGEL2005
74928-002-05HAND SANITIZER250 mL in 1 BOTTLEGEL2505
74928-002-06HAND SANITIZER500 mL in 1 BOTTLEGEL5005
74928-002-07HAND SANITIZER750 mL in 1 BOTTLEGEL7505
74928-002-08HAND SANITIZER1000 mL in 1 BOTTLEGEL10005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74928-002HAND SANITIZER GEL [SHANTOU WANLI BIOTECHNOLOGY CO.,LTD.]5Legacy NDC, 8 package rows20200603_a305d255-9668-0854-e053-2995a90ac5f9.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
74928-00274928-002-01, 74928-002-02, 74928-002-03, 74928-002-04, 74928-002-05, 74928-002-06, 74928-002-07, 74928-002-08

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
CARBOMER 1342809Y72KV36IACT
DIGLYCERIN3YC120743UIACT
WATER059QF0KO0RIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
CUPRIC TRIETHANOLAMINE6NU949U74EIACT
ALCOHOL3K9958V90MACTIB

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
a7177742-63f4-070d-e053-2a95a90a117ea305d255-9668-0854-e053-2995a90ac5f92020-06-02WarningsExact identifier
spl id: a7177742-63f4-070d-e053-2a95a90a117e
spl set id: a305d255-9668-0854-e053-2995a90ac5f9

Reported adverse events (FAERS/openFDA)#

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