Anti-Bacterial Hand Honolulu Sun: Package Insert and Label Information

ANTI-BACTERIAL HAND HONOLULU SUN- alcohol spray
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.

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

ANTI-BACTERIAL HAND HONOLULU SUN alcohol spray

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-6117 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (ALCOHOL) ALCOHOL 72 mL in 100 mL

Inactive Ingredients Ingredient Name Strength WATER

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:62670-6117-2 88 mL in 1 BOTTLE, PUMP None

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)

Revised: 06/2021 Bath & Body Works, Inc.