DRUG FACTS

Manufacturer: Bath & Body Works, Inc.
Effective date: 2019-06-19
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 22:59:48

Label at a glance#

ProductAnti-Bacterial Hand A Thousand Wishes

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, Calcium Sodium
Borosilicate, Propylene Glycol, Hydroxyethyl Urea,
Wheat Amino Acids, Tocopheryl Acetate, Glycerin,
Aloe Barbadensis Leaf Juice, Tin Oxide, Elaeis Guineensis
(Palm) Extract, Olea Europaea (Olive) Fruit Extract,
Honey Extract (Mel, Extrait de miel), Cocos Nucifera
(Coconut) Fruit Extract, Titanium Dioxide (CI 77891),
Red 33 (CI 17200), Yellow 5 (CI 19140),
Ext. Violet 2 (CI 60730).

PRODUCT PACKAGING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AB HG A Thousand Wishes

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1037039	ethanol 68 % Topical Gel	PSN	4
1037039	ethanol 0.68 ML/ML Topical Gel	SCD	4
1037039	ethanol 68 % Topical Gel	SY	4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62670-5643-0	2021-01-29	C162847	48780-1	ba0f9c33-1323-a910-e053-dadaa90a0b85	DRUG FACTS
62670-5643-1	2021-01-29	C162847	48780-1	ba0f9c33-1323-a910-e053-dadaa90a0b85	DRUG FACTS
62670-5643-3	2021-01-29	C162847	48780-1	ba0f9c33-1323-a910-e053-dadaa90a0b85	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
62670-5643-0	Anti-Bacterial Hand A Thousand Wishes	29 mL in 1 BOTTLE	GEL	29	4
62670-5643-1	Anti-Bacterial Hand A Thousand Wishes	73 mL in 1 BOTTLE	GEL	73	4
62670-5643-3	Anti-Bacterial Hand A Thousand Wishes	236 mL in 1 BOTTLE, PUMP	GEL	236	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62670-5643	ANTI-BACTERIAL HAND A THOUSAND WISHES (ALCOHOL) GEL [BATH & BODY WORKS, INC.]	4	Legacy NDC, 3 package rows	20190629_8154cf9d-e4e3-442e-8f52-6eb0d0798169.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 A Thousand Wishes
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62670-5643	62670-5643-0, 62670-5643-1, 62670-5643-3

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
8e389acf-f7c7-4720-af8a-bd1d02052f3b			8154cf9d-e4e3-442e-8f52-6eb0d0798169	2019-06-19	Warnings	Exact identifier spl id: 8e389acf-f7c7-4720-af8a-bd1d02052f3b spl set id: 8154cf9d-e4e3-442e-8f52-6eb0d0798169

Reported adverse events (FAERS/openFDA)#

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