ANTI-BACTERIAL HAND AROMATHERAPY STRESS RELIEF EUCALYPTUS SPEARMINT- alcohol gel

Anti-Bacterial Hand by

Drug Labeling and Warnings

Anti-Bacterial Hand by is a Otc medication manufactured, distributed, or labeled by Bath & Body Works, Inc., Knowlton Development Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol 68%

PURPOSE

Antiseptic

USE

Decreases 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), Aloe Barbadensis Leaf Juice, Honey Extract (Mel, Extrait de miel), Elaeis Guineensis (Palm) Extract, Cocos Nucifera (Coconut) Fruit Extract, Olea Europaea (Olive) Fruit Extract, Eucalyptus Globulus Leaf Oil, Mentha Viridis (Spearmint) Leaf Oil, Tocopheryl Acetate, Retinyl Palmitate, Glycerin, Carbomer, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Propylene Glycol, Hydroxyethyl Urea, Wheat Amino Acids, Hydroxypropyl Methylcellulose, Ultramarines (CI 77007), Yellow 5 (CI 19140), Red 40 (CI 16035), Blue 1 (CI 42090).

COMPANY INFORMATION

Bath & Body Works, Distr.

Reynoldsburg, Ohio 43068

1-800-395-1001

www.bathandbodyworks.com

PRODUCT PACKAGING

INGREDIENTS AND APPEARANCE

ANTI-BACTERIAL HAND  AROMATHERAPY STRESS RELIEF EUCALYPTUS SPEARMINT
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62670-4908
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	68 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62670-4908-0	29 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/06/2012

Labeler - Bath & Body Works, Inc. (878952845)

Establishment
Name	Address	ID/FEI	Business Operations
Knowlton Development Corporation		968939913	manufacture(62670-4908)