Anti-Bacterial Hand

Manufacturer
Bath & Body Works, Inc.
Effective date
2015-01-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:41:35

Label at a glance#

ProductAnti-Bacterial Hand Fresh Market Apple
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Spray hands thoroughly. Rub until dry.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol (72%)

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

To decrease bacteria on skin.

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.

KEEP OUT OF THE 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

  • Spray hands thoroughly.
  • Rub until dry.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water (Aqua, Eau), Aloe Barbadensis Leaf Juice, Cocos Nucifera (Coconut) Fruit Extract, Honey Extract (Mel, Extrait de miel), Olea Europaea (Olive) Fruit Extract, Tocopheryl Acetate,  Fragrance (Parfum), PEG-12 Dimethicone, Butylene Glycol, Butyl Methoxydibenzoylmethane, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Red 4 (CI 14700), Red 33 (CI 17200), Yellow 5 (CI 19140).

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
1425407ethanol 72 % Topical SprayPSN3
1425407ethanol 0.72 ML/ML Topical SpraySCD3
1425407ethanol 72 % Topical SpraySY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62670-4114-22020-01-31C16284748780-19d75b9d0-8644-f424-e053-dadaa90a57ced72975f8-2046-49e9-a6c6-eaf5e3dad1eb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62670-4114-2Anti-Bacterial HandFresh Market Apple56 mL in 1 BOTTLE, PUMPLIQUID563

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62670-4114ANTI-BACTERIAL HAND FRESH MARKET APPLE (ALCOHOL) LIQUID [BATH & BODY WORKS, INC.]3Legacy NDC, 1 package rows20150202_d72975f8-2046-49e9-a6c6-eaf5e3dad1eb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M3
ALCOHOLACTIVE MOIETY3K9958V90M3
WATERINACTIVE INGREDIENT059QF0KO0R3

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
62670-411462670-4114-2

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
fbed1660-25ae-4e98-9aee-370f6b91ac4dd72975f8-2046-49e9-a6c6-eaf5e3dad1eb2015-01-30WarningsExact identifier
spl id: fbed1660-25ae-4e98-9aee-370f6b91ac4d
spl set id: d72975f8-2046-49e9-a6c6-eaf5e3dad1eb

Reported adverse events (FAERS/openFDA)#

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