FDA.reportPublic FDA data

INSTANT HAND SANITIZER

Manufacturer
PERFECT MEDICS, INC | ZHEJIANG RIFESHOW COSMETICS CO.,LTD
Effective date
2020-09-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:29:13

Label at a glance#

ProductINSTANT HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

wet hand thoroughly and allow to dry without wiping for children under6, use only under adult supervision not recommended for infants

Storage and handling

do not store above 105℉; may discolor some fabrics harmful to wood finish and plastic

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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 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. 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 skin irritation develops. 
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops.

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

  • wet hand thoroughly and allow to dry without wiping
  • for children under6, use only under adult supervision
  • not recommended for infants

Other information

STORAGE AND HANDLING SECTION

do not store above 105℉;

may discolor some fabrics

harmful to wood finish and plastic

Inactive ingredients

INACTIVE INGREDIENT SECTION

DI water,glycerin, carbopol,triethanolamine,tocopheryl acetate,aloe barbadensis leaf juice

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Labelimage descriptionimage description image descriptionimage description image descriptionimage description image descriptionimage description image descriptionimage description image descriptionimage description

SPL UNCLASSIFIED SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79134-005-012023-07-28C16284748780-10191ceaa-7147-198a-e063-dbdaa90aec3e5930d0c0-4d9f-4876-a0fc-f7c20eea3f87
79134-005-022023-07-28C16284748780-10191ceaa-7147-198a-e063-dbdaa90aec3e5930d0c0-4d9f-4876-a0fc-f7c20eea3f87
79134-005-032023-07-28C16284748780-10191ceaa-7147-198a-e063-dbdaa90aec3e5930d0c0-4d9f-4876-a0fc-f7c20eea3f87

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79134-005-01INSTANT HAND SANITIZER29 mL in 1 BOTTLEGEL292
79134-005-02INSTANT HAND SANITIZER60 mL in 1 BOTTLEGEL602
79134-005-03INSTANT HAND SANITIZER3780 mL in 1 BOTTLEGEL37802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79134-005INSTANT HAND SANITIZER (ALCOHOL) GEL [PERFECT MEDICS, INC]2Legacy NDC, 3 package rows20200915_5930d0c0-4d9f-4876-a0fc-f7c20eea3f87.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
79134-00579134-005-01, 79134-005-02, 79134-005-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
POLYACRYLIC ACID (250000 MW)9G2MAD7J6WIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT

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
6dd8e091-dd23-4bce-ad2c-a797591ac79a5930d0c0-4d9f-4876-a0fc-f7c20eea3f872020-09-15WarningsExact identifier
spl id: 6dd8e091-dd23-4bce-ad2c-a797591ac79a
spl set id: 5930d0c0-4d9f-4876-a0fc-f7c20eea3f87

Reported adverse events (FAERS/openFDA)#

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