DrugInserts.com: Trustworthy FDA Drug Information

Over the Counter Medications

Package Insert and Label Information: Anti-Bacterial Hand Gel White Citrus

By Bath & Body Works, Inc. | Last revised: 1 January 2010

ANTI-BACTERIAL HAND GEL WHITE CITRUS- alcohol gel
Bath & Body Works, Inc.

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.

ACTIVE INGREDIENT

Alcohol 68%

PURPOSE

Antiseptic

USE

Decrease bacteria on hands.

WARNINGS

For external use only.

When using this product keep out of eyes. Stop use and ask a doctor if irritation or redness develops.

FLAMMABLE

Keep away from flame or high heat.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

  • Rub a dime sized drop into hands.

INACTIVE INGREDIENTS

Water (Aqua, Eau), Isopropyl Alcohol, Fragrance (Parfum), Honey Extract (Mel, Extrait de Miel), Elaeis Guineensis (Palm) Extract, Olea Europaea (Olive) Fruit Extract, Cocos Nucifera (Coconut) Fruit Extract, Wheat Amino Acids, Retinyl Palmitate, Tocopheryl Acetate, Glycerin, Carbomer, Cellulose, Hydroxyethyl Urea, Hydroxypropyl Methylcellulose, Lactose, Isopropyl Myristate, Propylene Glycol, Aminomethyl Propanol, Ultramarines (CI 77007), Yellow 5 (CI 19140), Yellow 6 (CI 15985), Blue 1 (CI 42090), Red 40 (CI 16035).

COMPANY INFORMATION

Bath & Body Works, Distr.
Reynoldsburg, Ohio 43068
1-800-395-1001
www.bathandbodyworks.com

PRODUCT PACKAGING

Front Label
(click image for full-size original)
Back Label
(click image for full-size original)
ANTI-BACTERIAL HAND GEL WHITE CITRUS
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-3642
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 68 mL in 100 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62670-3642-0 29 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333 01/01/2010
Labeler — Bath & Body Works, Inc. (878952845)

Revised: 01/2010 Bath & Body Works, Inc.