FDA.reportPublic FDA data

Anti-BacterialHandSpray

Manufacturer
Bath & Body Works, Inc. | KDC US Holdings, Inc.
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:47:07

Label at a glance#

ProductAnti-BacterialHandSpray Boardwalk Vanilla Cone
Active ingredientALCOHOL
Label structure12 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

Decreases bacteria on hands.

Warnings

WARNINGS SECTION

Flammable. Keep away from flame or high heat.

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor is irritation and redness develop.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray hands thoroughly.
  • Rub until dry.

INACTIVE INGREDIENT SECTION

Water (Aqua, Eau), Fragrance (Parfum), PEG-12 Dimethicone, Butyrospermum Parkii (Shea) Butter Extract, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Green 3 (CI 42053), Yellow 5 (CI 19140), Ext. Violet 2 (CI 60730).

SPL UNCLASSIFIED SECTION

Bath & Body Works Distr., 95 West Main Street

New Albany, OH 43054, 1-800-395-1001

pat. www.bbwinc.com/patents

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ABHS Boardwalk Vanilla ConeABHS Boardwalk Vanilla Cone

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1425407ethanol 72 % Topical SprayPSN1
1425407ethanol 0.72 ML/ML Topical SpraySCD1
1425407ethanol 72 % Topical SpraySY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62670-6799-0Anti-BacterialHandSprayBoardwalk Vanilla Cone29 mL in 1 BOTTLE, SPRAYSPRAY291

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62670-6799ANTI-BACTERIALHANDSPRAY BOARDWALK VANILLA CONE (ALCOHOL) SPRAY [BATH & BODY WORKS, INC.]1Current NDC, 1 package rows20241222_29a3b5b3-c104-7754-e063-6294a90af8e7.zip

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
62670-679962670-6799-0

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
WATER059QF0KO0RIACT
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
Anti-BacterialHandSpray Boardwalk Vanilla ConeALCOHOLBath & Body Works, Inc.29a3b5b3-c104-7754-e063-6294a90af8e72024-12-19WarningsExact identifier
ndc (package): 62670-6799-0
ndc (product): 62670-6799
ndc11 (package): 62670679900
spl id: 29a3af99-8187-9ec6-e063-6294a90ab842
spl set id: 29a3b5b3-c104-7754-e063-6294a90af8e7

Reported adverse events (FAERS/openFDA)#

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