Anti-Bacterial Hand Gel

Manufacturer
Bath & Body Works, Inc. | KDC US Holdings, Inc. | Memphis Contract Packaging
Effective date
2023-11-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:20:22

Label at a glance#

ProductAnti-Bacterial Hand Gel Pumpkin Cupcake
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Rub a dime sized drop into hands.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 71%

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 keep out of eyes. Stop use and ask a doctor if irritation or redness develops.

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

Rub a dime sized drop into hands.

INACTIVE INGREDIENT SECTION

Inactive Ingredients Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Carbomer, Aminomethyl Propanol, Isopropyl Myristate, Hydroxyethyl Urea, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Butyrospermum Parkii (Shea) Butter Extract, Red 40 (CI 16035), Yellow 5 (CI 19140), Blue 1 (CI 42090), Red 33 (CI 17200), 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

ABHG Pumpkin CupcakeABHG Pumpkin Cupcake

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62670-6573ANTI-BACTERIAL HAND GEL PUMPKIN CUPCAKE (ALCOHOL) GEL [BATH & BODY WORKS, INC.]1Unmatched20231121_0a970cb1-5167-e80c-e063-6294a90ac99b.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
62670-657362670-6573-0

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
0a96ff82-df59-91ed-e063-6394a90afed70a970cb1-5167-e80c-e063-6294a90ac99b2023-11-20WarningsExact identifier
spl id: 0a96ff82-df59-91ed-e063-6394a90afed7
spl set id: 0a970cb1-5167-e80c-e063-6294a90ac99b

Reported adverse events (FAERS/openFDA)#

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