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Anti-Bacterial Hand Spray Sea Island Cotton

Dosage form: liquid
Ingredients: ALCOHOL 72mL in 100mL
Labeler: Bath & Body Works, Inc.
NDC Code: 62670-3755

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.

DRUG FACTS

ACTIVE INGREDIENTAlcohol (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),  Fragrance (Parfum), Tocopheryl Acetate, PEG-12 Dimethicone, Butylene Glycol, Propylene Glycol, Butyl Methoxydibenzoylmethane, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Ext. Violet 2 (CI 60730), Yellow 5 (CI 19140), Blue 1 (CI 42090).

COMPANY INFORMATION

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


PRODUCT PACKAGING
ANTI-BACTERIAL HAND SPRAY  SEA ISLAND COTTON
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-3755
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL72 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ALOE VERA LEAF 
BLACK OLIVE 
COCONUT  
HONEY 
.ALPHA.-TOCOPHEROL ACETATE, D- 
DIMETHICONE 
PROPYLENE GLYCOL 
BUTYLENE GLYCOL 
AVOBENZONE 
OCTINOXATE 
OCTISALATE 
EXT. D&C VIOLET NO. 2 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:62670-3755-256 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/21/2010
Labeler - Bath & Body Works, Inc. (878952845)

Revised: 12/2010
 
Bath & Body Works, Inc.

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 combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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