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PURELL Waterless Surgical Scrub

Medically reviewed by Drugs.com. Last updated on Sep 22, 2021.

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

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-992
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage Description
1NDC:21749-992-0259 mL in 1 BOTTLE
2NDC:21749-992-331000 mL in 1 BOTTLE
3NDC:21749-992-891200 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/15/2011
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534MANUFACTURE(21749-992)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.088312414MANUFACTURE(21749-992), label(21749-992), pack(21749-992)

 
GOJO Industries, Inc.

Further information

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