ANTI-BACTERIAL HAND HONOLULU SUN- alcohol spray

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.. 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), Fragrance (Parfum), PEG-12 Dimethicone, Tocopheryl Acetate, Butyrospermum Parkii (Shea) Butter Extract, Aloe Barbadensis Leaf Juice, Propylene Glycol, 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  HONOLULU SUN
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62670-6117
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62670-6117-2	88 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/15/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/15/2021

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