Anti-Bacterial Hand Sanitizer by Bath & Body Works, Inc. / KDC US Holdings, Inc.

Anti-Bacterial Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

ANTI-BACTERIAL HAND SANITIZER AB HS BE WISE AND SANITIZE (FRESH RAINFALL)- alcohol gel 
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.

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ACTIVE INGREDIENT

Alcohol 71%

PURPOSE

Antiseptic

USE

Decrease bacteria on hands.

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 or increase.

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), Fragrance (Parfum), Carbomer, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Hydroxyethyl Urea, Propylene Glycol, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Hydroxypropyl Methylcellulose, Retinyl Palmitate, Ultramarines (CI 77007), Blue 1 (CI 42090), Yellow 5 (CI 19140), 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 SANITIZER  AB HS BE WISE AND SANITIZE (FRESH RAINFALL)
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62670-6056
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: 62670-6056-3	225 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/16/2021	12/16/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/16/2021	12/16/2021

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

Establishment
Name	Address	ID/FEI	Business Operations
KDC US Holdings, Inc.		792844680	manufacture(62670-6056)

Revised: 5/2013

Document Id: d4e4b669-f8da-41f6-b2a0-913bd6846d89

34390-5

Set id: 2ca3811c-175d-4107-961f-e2673cbd6d4a

Version: 1

Effective Time: 20130507