PURELL Waterless Surgical Scrub

Dosage form: liquid
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: GOJO Industries, Inc.
NDC code: 21749-992

Medically reviewed by Drugs.com. Last updated on Sep 23, 2024.

PURELL Waterless Surgical Scrub

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antiseptic surgical hand scrub

Uses

Significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care

Warnings

Flammable. Keep away from fire or flame.

For external use only

Sunburn Alert: This product contains an alpha hydroxy acid (AHA) that may increase the risk of sunburn. Take steps to limit sun exposure while using this product and for one week following use.

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

Stop use and ask a doctor if irritation and redness develop and persist 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

clean under the nails with a nail pick
mails should be maintained with a 1 millimeter free edge
place 2 mL of product into palm of one hand
dip fingers of opposite hand into the product and work under nails
spread remaining product evenly over the hands and lower 2/3 of one forearm paying particular attention to the nails, cuticles, and interdigital spaces
place 2 mL of product into opposite hand and repeat steps above
allow to air dry completely

Inactive ingredients

Water (Aqua), Isopropyl Myristate, Glycerin, Diisopropyl Sebacate, Citric Acid, PEG/PPG-20/6 Dimethicone, Tetradibutyl Pentaerythrityl Hydroxyhydrocinnamate, Hydroxypropylcellulose, Polyquaternium-37, Methylchloroisothiazolinone, Methylisothiazolinone

PURELL WATERLESS SURGICAL SCRUB
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-992
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	0.7 mL in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
ISOPROPYL ALCOHOL
ISOPROPYL MYRISTATE
GLYCERIN
DIISOPROPYL SEBACATE
CITRIC ACID MONOHYDRATE
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)
HYDROXYPROPYL CELLULOSE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE

Packaging
#	Item Code	Package Description
1	NDC:21749-992-02	59 mL in 1 BOTTLE
2	NDC:21749-992-33	1000 mL in 1 BOTTLE
3	NDC:21749-992-89	1200 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/15/2011

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		036424534	MANUFACTURE(21749-992)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		088312414	MANUFACTURE(21749-992), label(21749-992), pack(21749-992)

Revised: 10/2017

Document Id: fbeebc0d-12ed-4beb-89d5-c6389398d088

Set id: e3ed5e0c-1e21-47eb-a999-9c8aa5083dff

Version: 3

Effective Time: 20171002

GOJO Industries, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer