75% Alcohol Hand Sanitizer

Manufacturer
Shangrao Chunyu Technology Co.,ltd.
Effective date
2020-07-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:20:15

Label at a glance#

Product75% Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Deposit a dime size amount of product onto palm of hand. Rub hands together until dry.

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

For hand-washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

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

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.

Do not use

OTC - STOP USE SECTION

Stop use and ask doctor if irritation and redness develop.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or call Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Deposit a dime size amount of product onto palm of hand.
  • Rub hands together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aminomethylpropanol, carbopol 980 polymer, glycerin, propylene glycol, sterile distilled water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30mL NDC: 72922-014-01 Package LabelPackage Label Package LabelPackage Label

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL NDC: 72922-014-02 Package LabelPackage Label Package LabelPackage Label

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

​29 mL NDC: 72922-014-03 Package LabelPackage Label Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN2
1047755ethanol 0.75 ML/ML Topical SolutionSCD2
1047755ethanol 75 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72922-014-0175% Alcohol Hand Sanitizer30 mL in 1 BOTTLE, PLASTICSOLUTION302
72922-014-0275% Alcohol Hand Sanitizer60 mL in 1 BOTTLE, PLASTICSOLUTION602
72922-014-0375% Alcohol Hand Sanitizer29 mL in 1 BOTTLE, PLASTICSOLUTION292

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72922-01475% ALCOHOL HAND SANITIZER (HAND SANITIZER) SOLUTION [SHANGRAO CHUNYU TECHNOLOGY CO.,LTD.]2Legacy NDC, 3 package rows20200707_a95925df-bcf4-0306-e053-2a95a90accea.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
72922-01472922-014-01, 72922-014-02, 72922-014-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
a9d717fd-ea73-6af8-e053-2a95a90a0653a95925df-bcf4-0306-e053-2a95a90accea2020-07-07WarningsExact identifier
spl id: a9d717fd-ea73-6af8-e053-2a95a90a0653
spl set id: a95925df-bcf4-0306-e053-2a95a90accea

Reported adverse events (FAERS/openFDA)#

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