TRANSCEND ALCO-FOAM HAND SANITIZER- alcohol liquid

Transcend Alco-Foam Hand Sanitizer by

Drug Labeling and Warnings

Transcend Alco-Foam Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Von Drehle Corporation, Woodbine Products Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%v/v

Purpose

Sanitizer

Uses:

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

Warnings:

Flammable. Keep away from fire or flame

For external use only.

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

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

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

Directions:

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:

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

Inactive Ingredients:

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

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)

INGREDIENTS AND APPEARANCE

TRANSCEND ALCO-FOAM HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81792-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)
BUTYL ACRYLATE/METHYL METHACRYLATE/PERFLUOROHEXYLETHYL METHACRYLATE COPOLYMER (SALUS AF) (UNII: HLB263IJK9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81792-001-01	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/01/2023

Labeler - Von Drehle Corporation (071054415)

Establishment
Name	Address	ID/FEI	Business Operations
Woodbine Products Company		004220323	manufacture(81792-001)