FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Punch Studio, LLC | Ningbo Pretty Tourism Manufacture Co., Ltd.
Effective date
2022-01-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:46:38

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

TO HELP REDUCE BACTERIA ON HANDS WHEN WATER & SOAP ARE NOT AVAILABLE

Dosage and administration

APPLY AS NEEDED INTO PALM OF HANDS, RUB HANDS TOGETHER UNTIL DRY SUPERVISE CHILDREN UNDER 6 YEARS OLD

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

EHTANOL 62%. PURPOSE: ANTISEPTIC

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

  • TO HELP REDUCE BACTERIA ON HANDS
  • WHEN WATER & SOAP ARE NOT AVAILABLE

WARNINGS

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY
  • KEEP OUT OF EYES
  • FLAMMABLE, KEEP AWAY FROM HEAT OR FLAME

DO NOT USE

OTC - DO NOT USE SECTION

  • ON CHILDREN LESS THAN 2 YEARS OF AGE
  • ON OPEN SKIN WOUNDS

KEEP OUT OF REACK OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IF SWALLOWED, GET MEDICAL HELP OR CALL A POISON CONTROL VENTER RIGHT AWAY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • APPLY AS NEEDED INTO PALM OF HANDS, RUB HANDS TOGETHER UNTIL DRY
  • SUPERVISE CHILDREN UNDER 6 YEARS OLD

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, TRIETHANOLAMINE, CARBOMER, GLYCERIN, PROPYLENE GLYCOL, ALOE BARBADENSIS EXTRACT, TOCOPHERYL ACETATE

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

150 mL NDC: 75601-0001-1 Front & back labelsFront & back labels

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75601-0001-12023-07-28C16284748780-10191ceaa-6553-198a-e063-dbdaa90aec3eHand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75601-0001-1Hand Sanitizer150 mL in 1 BOTTLE, PUMPGEL1502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75601-0001HAND SANITIZER (ALCOHOL) GEL [PUNCH STUDIO, LLC]2Legacy NDC, 1 package rows20220113_a7aea13a-96aa-6c86-e053-2995a90a75de.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75601-000175601-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT

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
d56f9b98-0e35-2749-e053-2a95a90afa56a7aea13a-96aa-6c86-e053-2995a90a75de2022-01-12WarningsExact identifier
spl id: d56f9b98-0e35-2749-e053-2a95a90afa56
spl set id: a7aea13a-96aa-6c86-e053-2995a90a75de

Reported adverse events (FAERS/openFDA)#

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