Anti-Bacterial Hand

Manufacturer
Bath & Body Works, Inc. | Knowlton Development Corporation | Bocchi Laboratories | Accel inc.
Effective date
2015-06-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:42:44

Label at a glance#

ProductAnti-Bacterial Hand Japanese Cherry Blossom
Active ingredientALCOHOL
Label structure12 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

Decreases bacteria on hands.

WARNINGS

WARNINGS SECTION

For external use only.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

keep out of eyes.

STOP USE AND ASK A DOCTOR

OTC - STOP USE SECTION

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, Cocos Nucifera (Coconut) Fruit Extract, Olea Europaea (Olive) Fruit Extract, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Retinyl Palmitate, Glycerin, Wheat Amino Acids, Carbomer, Propylene Glycol, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Hydroxyethyl Urea, Hydroxypropyl Methylcellulose, Ultramarines (CI 77007), Red 40 (CI 16035), Red 33 (CI 17200), Ext. Violet 2 (CI 60730).

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

MM1MM1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1037039ethanol 68 % Topical GelPSN1
1037039ethanol 0.68 ML/ML Topical GelSCD1
1037039ethanol 68 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62670-4915-02020-01-31C16284748780-19d75b9d0-f718-f424-e053-dadaa90a57ce9ba1c43c-ef1a-4da4-ad3e-a5ec2e5e989d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62670-4915-0Anti-Bacterial HandJapanese Cherry Blossom29 mL in 1 BOTTLEGEL291

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62670-4915ANTI-BACTERIAL HAND JAPANESE CHERRY BLOSSOM (ALCOHOL) GEL [BATH & BODY WORKS, INC.]1Legacy NDC, 1 package rows20150611_9ba1c43c-ef1a-4da4-ad3e-a5ec2e5e989d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62670-491562670-4915-0

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
404eee04-fa79-4c5d-be16-d0830767a7bb9ba1c43c-ef1a-4da4-ad3e-a5ec2e5e989d2015-06-10WarningsExact identifier
spl id: 404eee04-fa79-4c5d-be16-d0830767a7bb
spl set id: 9ba1c43c-ef1a-4da4-ad3e-a5ec2e5e989d

Reported adverse events (FAERS/openFDA)#

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