Advanced Hand Sanitizer Foam with Aloe

Manufacturer
DEALMED MEDICAL SUPPLIES LLC | PELICAN GROUP LLC, THE
Effective date
2022-02-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:48:07

Label at a glance#

ProductAdvanced Hand Sanitizer Foam with Aloe
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

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

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin that can cause disease. recommended for repeat use

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame, For external use only.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On open skin wounds

OTC - WHEN USING SECTION

Do not use in or near the eyes. in case of contact, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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 thorougly cover your hands. Rub hands together until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-12 Dimethicone, Carprylyl Glycol, Aloe Vera, Glycerin, Fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Foam Hand SanitizerFoam Hand Sanitizer473.2 mL NDC: 78257-916-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN2
616805ethanol 0.7 ML/ML Topical FoamSCD2
616805ethanol 70 % Topical FoamSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78257-916-012023-07-28C16284748780-10191ceaa-6f93-198a-e063-dbdaa90aec3eb9e6f96b-ad06-e89f-e053-2995a90ab942

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78257-916-01Advanced Hand Sanitizer Foam with Aloe473.2 mL in 1 BOTTLE, PUMPSOLUTION473.22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78257-916ADVANCED HAND SANITIZER FOAM WITH ALOE (ALCOHOL) SOLUTION [DEALMED MEDICAL SUPPLIES LLC]2Legacy NDC, 1 package rows20220207_b9e6f96b-ad06-e89f-e053-2995a90ab942.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
78257-91678257-916-01

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
d75e84c0-470a-4dcb-e053-2995a90ae9c9b9e6f96b-ad06-e89f-e053-2995a90ab9422022-02-06WarningsExact identifier
spl id: d75e84c0-470a-4dcb-e053-2995a90ae9c9
spl set id: b9e6f96b-ad06-e89f-e053-2995a90ab942

Reported adverse events (FAERS/openFDA)#

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