DRUG FACTS

Manufacturer
Bath & Body Works, Inc.
Effective date
2010-01-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:28:18

Label at a glance#

ProductAnti-Bacterial Hand Warm Vanilla Sugar
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Rub a dime sized drop into hands.

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), Honey Extract (Mel, Extrait de Miel), Elaeis Guineensis (Palm) Extract,  Olea Europaea (Olive) Fruit Extract, Cocos Nucifera (Coconut) Fruit Extract, Wheat Amino Acids, Retinyl Palmitate, Tocopheryl Acetate, Glycerin, Carbomer, Cellulose, Hydroxyethyl Urea, Hydroxypropyl Methylcellulose, Lactose, Isopropyl Myristate, Propylene Glycol, Aminomethyl Propanol, Ultramarines (CI 77007), Yellow 5 (CI 19140), Red 33 (CI 17200), Blue 1 (CI 42090).

COMPANY INFORMATION

SPL UNCLASSIFIED SECTION

Bath & Body Works, Distr.
Reynoldsburg, Ohio 43068
1-800-395-1001
www.bathandbodyworks.com

PRODUCT PACKAGING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front Label
Front Label
Back Label
Back Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1037039ethanol 68 % Topical GelPSN2
1037039ethanol 0.68 ML/ML Topical GelSCD2
1037039ethanol 68 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62670-3643-02019-10-29C16284748780-1960f7f55-c36b-8e05-e053-dbdaa90a074aDRUG FACTS
62670-3643-12019-10-29C16284748780-1960f7f55-c36b-8e05-e053-dbdaa90a074aDRUG FACTS
62670-3643-32019-10-29C16284748780-1960f7f55-c36b-8e05-e053-dbdaa90a074aDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62670-3643-0Anti-Bacterial Hand Warm Vanilla Sugar29 mL in 1 BOTTLEGEL292
62670-3643-1Anti-Bacterial Hand Warm Vanilla Sugar73 mL in 1 BOTTLEGEL732
62670-3643-3Anti-Bacterial Hand Warm Vanilla Sugar236 mL in 1 BOTTLE, PUMPGEL2362

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62670-3643ANTI-BACTERIAL HAND (ALCOHOL) GEL [BATH & BODY WORKS, INC.]2Legacy NDC, 3 package rows20110615_b23e9602-36ea-408e-b367-026795779024.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M2
ALCOHOLACTIVE MOIETY3K9958V90M2

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62670-364362670-3643-0, 62670-3643-1, 62670-3643-3

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6f2ed26c-6478-496d-bb32-7994df3e3e7bb23e9602-36ea-408e-b367-0267957790242010-01-01WarningsExact identifier
spl id: 6f2ed26c-6478-496d-bb32-7994df3e3e7b
spl set id: b23e9602-36ea-408e-b367-026795779024

Reported adverse events (FAERS/openFDA)#

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