PURELL Waterless Surgical Scrub
Dosage form: liquid
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-992
Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
with Moisturizers
Ethyl alcohol 70% v/v
Antiseptic surgical hand scrub
Significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care
Flammable. Keep away from fire or flame.
For external use only
Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
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.
Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.
If swallowed, get medical help or contact a Poison Control Center right away.
- 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
- Store below 110°F (43°C)
- May discolor certain fabrics or surfaces
Water (Aqua), Isopropyl Myristate, Glycerin, Diisopropyl Sebacate, Citric Acid, PEG/PPG-20/6 Dimethicone, Tetradibutyl Pentaerythrityl Hydroxyhydrocinnamate, Hydroxypropylcellulose, Polyquaternium-37, Methylchloroisothiazolinone, Methylisothiazolinone
Call 1-800-321-9647 Monday through Friday 8:30 AM to 5:00 PM
PURELL
SURGICAL SCRUB
with MOISTURIZERS
Not for Retail Sale
2 FL OZ 59 mL
Bottle Label
| PURELL WATERLESS SURGICAL SCRUB
alcohol liquid |
||||||||||||||||||||||||
|
||||||||||||||||||||||||
|
||||||||||||||||||||||||
|
||||||||||||||||||||||||
|
||||||||||||||||||||||||
|
||||||||||||||||||||||||
| Labeler - GOJO Industries, Inc. (004162038) |
| Establishment | |||
| Name | Address | ID/FEI | Operations |
| GOJO Industries, Inc. | 004162038 | MANUFACTURE(21749-992) | |
Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.
