PURELL Advanced Hand Sanitizer Winterberry Delight description, usages, side effects, indications, overdosage, supplying and lots more!

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PURELL Advanced Hand Sanitizer Winterberry Delight

GOJO Industries, Inc.

PURELL Advanced Hand Sanitizer Winterberry Delight


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient


Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if irritation or rash appears and lasts.

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

PURELL Advanced Hand Sanitizer Winterberry Delight Other information

Store below 110°F (43°C)

May discolor certain fabrics or surfaces

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Caprylyl glycol, Glycerin, Isopropyl Myristate, Lactose, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Cellulose, Hydroxypropyl Methylcellulose, Fragrance (Parfum), Blue 1 (CI 42090), Red 33 (CI 17200), Ultramarines (CI 77007), Yellow 5 (CI 19140)

Package/Label


PURELL Advanced Hand Sanitizer Winterberry Delight

Kills the Most Germs* *Ounce for ounce kills outperforms PURELL Original formulations when used on hands as directed

Kills more than 99.99% of most common germs that may make you sick


Distributed by:

GOJO Industries, Inc.

Akron, OH 44309

Questions? Tel: 1-888-4-PURELL www.PURELL.com

(C) 2012. GOJO Industries, Inc.

All rights reserved. Made in U.S.A.


Patent Pending

PURELL Advanced Hand Sanitizer Winterberry Delight


PURELL Advanced Hand Sanitizer Winterberry Delight

ALCOHOL GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21749-250
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 0.7 mL

Inactive Ingredients

Ingredient Name Strength
water
ISOPROPYL ALCOHOL
CAPRYLYL GLYCOL
GLYCERIN
ISOPROPYL MYRISTATE
LACTOSE
.ALPHA.-TOCOPHEROL ACETATE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
Aminomethylpropanol
POWDERED CELLULOSE
HYPROMELLOSES
FD&C BLUE NO. 1
D&C RED NO. 33
Ultramarine Blue
FD&C YELLOW NO. 5

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21749-250-01 30 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2012-11-01


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