Anti-Bacterial Hand Sanitizer

Manufacturer: Bath & Body Works, Inc. | Knowlton Development Corporation
Effective date: 2013-05-15
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:35:37

Label at a glance#

ProductAnti-Bacterial Hand Sanitizer Summer Escape

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

Rub a dime sized drop into hands.

Contacts and useful links#

PhoneLabel contact1-800-395-1001

Websitewww.bathandbodyworks.com

www.bathandbodyworks.com

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 68%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

Decrease bacteria on hands.

WARNINGS

WARNINGS SECTION

For external use only.

FLAMMABLE

WARNINGS AND PRECAUTIONS SECTION

Keep away from flame or high heat.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

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

STOP USE AND ASK A DOCTOR

OTC - STOP USE SECTION

if irritation and redness develop or increase.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Rub a dime sized drop into hands.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water (Aqua, Eau), Isopropyl Alcohol, Fragrance (Parfum), Honey Extract (Mel, Extrait de miel), Elaeis Guineensis (Palm) Extract, Cocos Nucifera (Coconut) Fruit Extract, Olea Europaea (Olive) Fruit Extract, Tocopheryl Acetate, Wheat Amino Acids, Retinyl Palmitate, Carbomer, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Hydroxyethyl Urea, Propylene Glycol, Hydroxypropyl Methylcellulose, Glycerin, Ultramarines (CI 77007), Red 33 (CI 17200), Blue 1 (CI 42090).

PRODUCT PACKAGING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MM1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1037039	ethanol 68 % Topical Gel	PSN	1
1037039	ethanol 0.68 ML/ML Topical Gel	SCD	1
1037039	ethanol 68 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62670-4564-3	2019-11-27	C162847	48780-1	9855d018-dd63-cd31-e053-dbdaa90ab51a	525437ae-b205-4e12-aee3-9ef9e2000570

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62670-4564-3	Anti-Bacterial Hand SanitizerSummer Escape	225 mL in 1 BOTTLE, PUMP	GEL	225		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62670-4564	ANTI-BACTERIAL HAND SANITIZER SUMMER ESCAPE (ALCOHOL) GEL [BATH & BODY WORKS, INC.]	1	Legacy NDC, 1 package rows	20130603_525437ae-b205-4e12-aee3-9ef9e2000570.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	1
ALCOHOL	ACTIVE MOIETY	3K9958V90M	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Anti-Bacterial Hand Sanitizer Summer Escape
Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62670-4564	62670-4564-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
245cff5b-e7b6-446b-9d32-b3680f7eebdb			525437ae-b205-4e12-aee3-9ef9e2000570	2013-05-15	Warnings	Exact identifier spl id: 245cff5b-e7b6-446b-9d32-b3680f7eebdb spl set id: 525437ae-b205-4e12-aee3-9ef9e2000570

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.