Perisol Hand Sanitizer Foam

Manufacturer
PELICAN GROUP LLC, THE
Effective date
2021-03-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:56

Label at a glance#

ProductPerisol Hand Sanitizer Foam
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 110F (43C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antimicrobial. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

  • Flammable. Keep away from fire or flame.
  • For external use only.

Do not use

OTC - DO NOT USE SECTION

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

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 in your palm to thoroughly cover your hands. Rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110F (43C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-12 Dimethicone, Caprylyl Glycol, Aloe Vera, Glycerin, Fragrance (Parfum)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Perisol Ultra moisturizing Hand Sanitizer FoamPerisol Ultra moisturizing Hand Sanitizer Foam473.2mL NDC: 44672-112-11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44672-112-112023-01-30C16284748780-1f386c649-ea07-0266-e053-dadaa90a7c1abd36ff51-cc1e-10b5-e053-2995a90ae50a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44672-112-11Perisol Hand Sanitizer Foam473.2 mL in 1 BOTTLE, PUMPSOLUTION473.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44672-112PERISOL HAND SANITIZER FOAM (ALCOHOL) SOLUTION [PELICAN GROUP LLC, THE]1Legacy NDC, 1 package rows20210312_bd36ff51-cc1e-10b5-e053-2995a90ae50a.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
44672-11244672-112-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
bd36fce8-a2cb-fd35-e053-2995a90a9d4fbd36ff51-cc1e-10b5-e053-2995a90ae50a2021-03-10WarningsExact identifier
spl id: bd36fce8-a2cb-fd35-e053-2995a90a9d4f
spl set id: bd36ff51-cc1e-10b5-e053-2995a90ae50a

Reported adverse events (FAERS/openFDA)#

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