75% Hand Sanitizer

Manufacturer
Shandong Retouch Wash And Sterilize Technology Co.,ltd.
Effective date
2023-02-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:53:59

Label at a glance#

Product75% Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Take 3mL of the product to moisten your hands and rub for 1 min until the liquid covers your hands, wait until dry, and no need to wash with water.

Storage and handling

Store in a cool, dry place (below 86F). Keep sealed. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

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 or if allergy to alcohol

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.

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

Take 3mL of the product to moisten your hands and rub for 1 min until the liquid covers your hands, wait until dry, and no need to wash with water.

Other information

STORAGE AND HANDLING SECTION

Store in a cool, dry place (below 86F). Keep sealed.

Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Triethanolamine, Emollients, Essence and purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL NDC:75532-001-01

PDPPDP

250 mL NDC:75532-001-02

PDPPDP

500 mL NDC:75532-001-03

PDPPDP

1000 mL NDC:75532-001-04

PDPPDP4000 mL NDC:75532-001-05

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN4
1305100ethanol 0.75 ML/ML Topical GelSCD4
1305100ethanol 75 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75532-001-0175% Hand Sanitizer60 mL in 1 BOTTLEGEL604
75532-001-0275% Hand Sanitizer250 mL in 1 BOTTLEGEL2504
75532-001-0375% Hand Sanitizer500 mL in 1 BOTTLEGEL5004
75532-001-0475% Hand Sanitizer1000 mL in 1 BOTTLEGEL10004
75532-001-0575% Hand Sanitizer4000 mL in 1 BOTTLEGEL40004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75532-00175% HAND SANITIZER (ALCOHOL) GEL [SHANDONG RETOUCH WASH AND STERILIZE TECHNOLOGY CO.,LTD.]4Legacy NDC, 5 package rows20230212_a3d95773-5f36-4f79-e053-2a95a90a131d.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75532-00175532-001-01, 75532-001-02, 75532-001-03, 75532-001-04, 75532-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
f463841d-aa9a-70b9-e053-2995a90a88f2a3d95773-5f36-4f79-e053-2a95a90a131d2023-02-10WarningsExact identifier
spl id: f463841d-aa9a-70b9-e053-2995a90a88f2
spl set id: a3d95773-5f36-4f79-e053-2a95a90a131d

Reported adverse events (FAERS/openFDA)#

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