FDA.reportPublic FDA data

Anti-Bacterial Hand

Manufacturer
Bath & Body Works, Inc. | Knowlton Development Corporation
Effective date
2019-06-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:19:53

Label at a glance#

ProductAnti-Bacterial Hand Georgia Peach
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), Carbomer, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Propylene Glycol, Hydroxyethyl Urea, Wheat Amino Acids, Tocopheryl Acetate, Retinyl Palmitate, Glycerin, Hydroxypropyl Methylcellulose, Aloe Barbadensis Leaf Juice, Elaeis Guineensis (Palm) Extract, Honey Extract (Mel, Extrait de miel), Olea Europaea (Olive) Fruit Extract, Cocos Nucifera (Coconut) Fruit Extract, Ultramarines (CI 77007), Yellow 6 (CI 15985), Red 33 (CI 17200), Yellow 5 (CI 19140), Red 40 (CI 16035), 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

ABHG Georgia PeachABHG Georgia Peach

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
62670-561462670-5614-0

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
8336679b-98f7-4956-8f54-6506e55abbf1ae6712ed-9c72-4253-818f-cb6bf261e90f2019-06-25WarningsExact identifier
spl id: 8336679b-98f7-4956-8f54-6506e55abbf1
spl set id: ae6712ed-9c72-4253-818f-cb6bf261e90f

Reported adverse events (FAERS/openFDA)#

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