Anti-Bacterial Hand

Manufacturer
Bath & Body Works, Inc.
Effective date
2020-05-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:26:25

Label at a glance#

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

AB HS Citrus & SunshineAB HS Citrus & Sunshine

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
62670-585562670-5855-2

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
6c54008f-7c4d-4797-98db-ebbc330e8899fae1ea23-1505-4e72-a42e-0fc12e9de2032020-05-26WarningsExact identifier
spl id: 6c54008f-7c4d-4797-98db-ebbc330e8899
spl set id: fae1ea23-1505-4e72-a42e-0fc12e9de203

Reported adverse events (FAERS/openFDA)#

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