ANTI-BACTERIAL HAND SPRAY SWEET PEA- alcohol liquid

Anti-Bacterial Hand Spray by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol (72%)

PURPOSE

Antiseptic

USE

To decrease bacteria on skin.

WARNINGS

For external use only.

FLAMMABLE

Keep away from flame or high heat.

WHEN USING THIS PRODUCT

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

STOP USE AND ASK A DOCTOR

if irritation and redness develop.

KEEP OUT OF THE REACH OF CHILDREN

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

DIRECTIONS

• Spray hands thoroughly.
  
• Rub until dry.
  

INACTIVE INGREDIENTS

Water (Aqua, Eau), Aloe Barbadensis Leaf Juice, Olea Europaea (Olive) Fruit Extract, Cocos Nucifera (Coconut) Fruit Extract, Honey Extract (Mel, Extrait de Miel), Tocopheryl Acetate,  Fragrance (Parfum), PEG-12 Dimethicone, Propylene Glycol, Butylene Glycol, Butyl Methoxydibenzoylmethane, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Yellow 5 (CI 19140), Red 33 (CI 17200), Ext. Violet 2 (CI 60730).

COMPANY INFORMATION

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

PRODUCT PACKAGING

INGREDIENTS AND APPEARANCE

ANTI-BACTERIAL HAND SPRAY  SWEET PEA
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62670-3756
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BLACK OLIVE (UNII: 2M6QWV94OC)
COCONUT (UNII: 3RT3536DHY)
HONEY (UNII: Y9H1V576FH)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
DIMETHICONE (UNII: 92RU3N3Y1O)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
AVOBENZONE (UNII: G63QQF2NOX)
OCTINOXATE (UNII: 4Y5P7MUD51)
OCTISALATE (UNII: 4X49Y0596W)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62670-3756-2	56 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/21/2010

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