FDA.reportPublic FDA data

Anti-Bacterial Hand WINTER CANDY APPLE - Bath & Body Works, Inc. | MCP TN

Manufacturer
Bath & Body Works, Inc. | MCP TN
Effective date
2022-12-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:42:07

Label at a glance#

ProductAnti-Bacterial Hand WINTER CANDY APPLE
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Rub a dime sized drop into hands.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

Decrease bacteria on hands.

WARNINGS SECTION

Flammable: Keep away from flame or high heat.

WARNINGS AND PRECAUTIONS SECTION

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

WARNINGS AND PRECAUTIONS SECTION

Stop use and ask a doctor if irritation and redness develop
or increase.

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), Fragrance (Parfum), Dimethicone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Isopropyl Myristate, Hydroxypropylcellulose, Aminomethyl Propanol, Lactose, Cellulose, Dimethiconol, Laureth-4, Laureth-23, Tocopheryl Acetate, Butyrospermum Parkii (Shea) Butter Extract, Aloe Barbadensis Leaf Juice, Retinyl Palmitate, Hydroxypropyl Methylcellulose, Titanium Dioxide (CI 77891), Ultramarines (CI 77007).

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

ABMHS WINTER CANDY APPLEABMHS WINTER CANDY APPLE

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
62670-652162670-6521-0

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
9ad0d07f-efbb-4793-a7cf-af0529308fc3fb818f55-b98b-4954-b96e-e53265aff8102022-12-20WarningsExact identifier
spl id: 9ad0d07f-efbb-4793-a7cf-af0529308fc3
spl set id: fb818f55-b98b-4954-b96e-e53265aff810

Reported adverse events (FAERS/openFDA)#

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