Anti-Bacterial Hand Sanitizer

Manufacturer: Bath & Body Works, Inc. | KDC US Holdings, Inc.
Effective date: 2021-06-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:41:00

Label at a glance#

ProductAnti-Bacterial Hand Sanitizer Black Cherry Merlot

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 71%

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

INACTIVE INGREDIENTS: Water (Aqua, Eau), Fragrance (Parfum), Carbomer, Lactose, Propylene Glycol, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Hydroxypropyl Methylcellulose, Retinyl Palmitate, Ultramarines (CI 77007), Red 33 (CI 17200), Ext. Violet 2 (CI 60730), Yellow 5 (CI 19140).

PRODUCT PACKAGING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AB HS Black Cherry Merlot

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62670-6062-3	2023-01-30	C162847	48780-1	c7ccaba7-2094-fd44-e053-dadaa90aa01b	cb2bb6e7-c10a-4c5c-acce-d3f66aff6948
62670-6062-3	2021-11-14	C162847	48780-1	c7ccaba7-2094-fd44-e053-dadaa90aa01b	cb2bb6e7-c10a-4c5c-acce-d3f66aff6948
62670-6062-3	2021-07-23	C162847	48780-1	c7ccaba7-2094-fd44-e053-dadaa90aa01b	cb2bb6e7-c10a-4c5c-acce-d3f66aff6948

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62670-6062-3	Anti-Bacterial Hand SanitizerBlack Cherry Merlot	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
62670-6062	ANTI-BACTERIAL HAND SANITIZER BLACK CHERRY MERLOT (ALCOHOL) GEL [BATH & BODY WORKS, INC.]	1	Legacy NDC, 1 package rows	20210623_cb2bb6e7-c10a-4c5c-acce-d3f66aff6948.zip

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 Black Cherry Merlot
Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62670-6062	62670-6062-3

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
02e23ba4-6dfe-4d2b-942c-ad488816fa0a			cb2bb6e7-c10a-4c5c-acce-d3f66aff6948	2021-06-17	Warnings	Exact identifier spl id: 02e23ba4-6dfe-4d2b-942c-ad488816fa0a spl set id: cb2bb6e7-c10a-4c5c-acce-d3f66aff6948

Reported adverse events (FAERS/openFDA)#

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