FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Shantou Aoxiangqi Daily Chemical Co., Ltd.
Effective date
2020-04-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:19

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 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 15-30°C (59-86°F) Avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand sterilize gel 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.

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 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-40 castor oil, Carbomer, Triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 ml NDC: 75234-237-01

100 ml NDC: 75234-237-02

250 ml NDC: 75234-237-03

300 ml NDC: 75234-237-04

500 ml NDC: 75234-237-05

800 ml NDC: 75234-237-06

1000 ml NDC: 75234-237-07

PRINCIPAL DISPLAY PANELPRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL 2PRINCIPAL DISPLAY PANEL 2

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
75234-237-012021-07-23C16284748780-1c7ccaba7-1ac7-fd44-e053-dadaa90aa01ba32500e9-ef7c-2a77-e053-2995a90a9d32
75234-237-022021-07-23C16284748780-1c7ccaba7-1ac7-fd44-e053-dadaa90aa01ba32500e9-ef7c-2a77-e053-2995a90a9d32
75234-237-032021-07-23C16284748780-1c7ccaba7-1ac7-fd44-e053-dadaa90aa01ba32500e9-ef7c-2a77-e053-2995a90a9d32
75234-237-042021-07-23C16284748780-1c7ccaba7-1ac7-fd44-e053-dadaa90aa01ba32500e9-ef7c-2a77-e053-2995a90a9d32
75234-237-052021-07-23C16284748780-1c7ccaba7-1ac7-fd44-e053-dadaa90aa01ba32500e9-ef7c-2a77-e053-2995a90a9d32
75234-237-062021-07-23C16284748780-1c7ccaba7-1ac7-fd44-e053-dadaa90aa01ba32500e9-ef7c-2a77-e053-2995a90a9d32
75234-237-072021-07-23C16284748780-1c7ccaba7-1ac7-fd44-e053-dadaa90aa01ba32500e9-ef7c-2a77-e053-2995a90a9d32

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75234-237-01Hand Sanitizer60 mL in 1 BOTTLEGEL601
75234-237-02Hand Sanitizer100 mL in 1 BOTTLEGEL1001
75234-237-03Hand Sanitizer250 mL in 1 BOTTLEGEL2501
75234-237-04Hand Sanitizer300 mL in 1 BOTTLEGEL3001
75234-237-05Hand Sanitizer500 mL in 1 BOTTLEGEL5001
75234-237-06Hand Sanitizer800 mL in 1 BOTTLEGEL8001
75234-237-07Hand Sanitizer1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75234-237HAND SANITIZER (ALCOHOL) GEL [SHANTOU AOXIANGQI DAILY CHEMICAL CO., LTD.]1Legacy NDC, 7 package rows20200415_a32500e9-ef7c-2a77-e053-2995a90a9d32.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75234-23775234-237-02, 75234-237-01, 75234-237-03, 75234-237-04, 75234-237-05, 75234-237-06, 75234-237-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
PEG-40 CASTOR OIL4ERD2076EFIACT
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
a324f6f7-a847-270d-e053-2a95a90a6233a32500e9-ef7c-2a77-e053-2995a90a9d322020-04-12WarningsExact identifier
spl id: a324f6f7-a847-270d-e053-2a95a90a6233
spl set id: a32500e9-ef7c-2a77-e053-2995a90a9d32

Reported adverse events (FAERS/openFDA)#

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