Transcend Alco-Foam Hand Sanitizer

Manufacturer
Von Drehle Corporation | Woodbine Products Company
Effective date
2024-03-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:09:37

Label at a glance#

ProductTranscend Alco-Foam Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin that can cause disease. Recommended for repeated use.

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%v/v

Purpose

OTC - PURPOSE SECTION

Sanitizer

Uses:

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin that can cause disease. Recommended for repeated use.

Warnings:

WARNINGS SECTION

Flammable. Keep away from fire or flame

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritationor redness develops, or if condition persists for more than 72 hours.

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:

OTHER SAFETY INFORMATION

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aqua, Acrylates/Perfluorohexylethyl Methacrylate Copolymer (and) Perfluorohexylethyl Alcohol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TRANSCEND

by Marcal

ALCO-FOAM HAND SANITIZER

Manufactured for Marcal Paper

QUESTIONS

Call 800-438-3631 or visit us online at marcalpaper.com

1

PET

Item #T740AS

1250 ml (42 fl. oz.)

Made in the U.S.A.

NSF

Nonfood Compounds

Program Listed (E3)

(Registration #161161)

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616763ethanol 62 % Topical FoamPSN1
616763ethanol 0.62 ML/ML Topical FoamSCD1
616763ethanol 62 % Topical FoamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81792-001-01Transcend Alco-Foam Hand Sanitizer1250 mL in 1 BOTTLELIQUID12501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81792-001TRANSCEND ALCO-FOAM HAND SANITIZER (ALCOHOL) LIQUID [VON DREHLE CORPORATION]1Current NDC, 1 package rows20240310_132b4d76-e08f-b359-e063-6394a90a95d4.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81792-00181792-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
Transcend Alco-Foam Hand SanitizerALCOHOLVon Drehle Corporation132b4d76-e08f-b359-e063-6394a90a95d42024-03-08WarningsExact identifier
ndc (package): 81792-001-01
ndc (product): 81792-001
ndc11 (package): 81792000101
spl id: 132b4d76-e090-b359-e063-6394a90a95d4
spl set id: 132b4d76-e08f-b359-e063-6394a90a95d4

Reported adverse events (FAERS/openFDA)#

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