DRUG FACTS

Manufacturer: Bath & Body Works, Inc.
Effective date: 2019-06-19
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: legacy-cache
Hydrated at: 2026-08-02 00:19:51

Label at a glance#

ProductAnti-Bacterial Hand Berry Galactic Swirl

Active ingredientALCOHOL

Label structure10 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.

When using this product keep out of eyes. Stop use and ask a doctor if irritation or redness develops.

FLAMMABLE

WARNINGS AND PRECAUTIONS SECTION

Keep away from flame or high heat.

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), Carbomer, Aminomethyl
Propanol, Isopropyl Myristate, Propylene Glycol, Calcium
Sodium Borosilicate, Hydroxyethyl Urea, Wheat Amino
Acids, Tocopheryl Acetate, Glycerin, Aloe Barbadensis
Leaf Juice, Tin Oxide, Elaeis Guineensis (Palm) Extract,
Cocos Nucifera (Coconut) Fruit Extract, Honey Extract
(Mel, Extrait de miel), Olea Europaea (Olive)
Fruit Extract, Titanium Dioxide (CI 77891),
Ext. Violet 2 (CI 60730), Yellow 5 (CI 19140).

PRODUCT PACKAGING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AB HG Berry Galactic Swirl

Products#

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

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

Anti-Bacterial Hand Berry Galactic Swirl
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62670-5639	62670-5639-0, 62670-5639-1, 62670-5639-3

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
02f77d5d-fdfd-4a63-85e5-637fd82eaded			a04ffa8a-e072-4d35-954e-9bff9f1e298d	2019-06-19	Warnings	Exact identifier spl id: 02f77d5d-fdfd-4a63-85e5-637fd82eaded spl set id: a04ffa8a-e072-4d35-954e-9bff9f1e298d

Reported adverse events (FAERS/openFDA)#

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