FDA.reportPublic FDA data

75% alcohol hand sanitizer

Manufacturer
JASPERS GLOBAL MANUFACTURING INC | Aogrand International Trade Corporation
Effective date
2023-02-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:54:03

Label at a glance#

Product75% alcohol hand sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping. for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic. Hand senitizer

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable. Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops
  • condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep it out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping.
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information

OTHER SAFETY INFORMATION

  • do not store above 105F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylic acid polymer, triethanolamine, water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500mL NDC: 75617-002-01

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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75617-002-012024-07-30C16284748780-1f386c649-dd42-0266-e053-dadaa90a7c1a75% alcohol hand sanitizer
75617-002-012024-01-30C16284748780-1f386c649-dd42-0266-e053-dadaa90a7c1a75% alcohol hand sanitizer
75617-002-012023-02-13C16284748780-1f386c649-dd42-0266-e053-dadaa90a7c1a75% alcohol hand sanitizer
75617-002-012023-01-30C16284748780-1f386c649-dd42-0266-e053-dadaa90a7c1a75% alcohol hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75617-002-0175% alcohol hand sanitizer500 mL in 1 BOTTLEGEL5004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75617-00275% ALCOHOL HAND SANITIZER (ALCOHOL) GEL [JASPERS GLOBAL MANUFACTURING INC]4Legacy NDC, 1 package rows20230214_a656c08e-31af-64b7-e053-2a95a90ad169.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
75617-00275617-002-01
74621-008

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
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
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
f48f636b-2136-e5a3-e053-2995a90a04d8a656c08e-31af-64b7-e053-2a95a90ad1692023-02-13WarningsExact identifier
spl id: f48f636b-2136-e5a3-e053-2995a90a04d8
spl set id: a656c08e-31af-64b7-e053-2a95a90ad169

Reported adverse events (FAERS/openFDA)#

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