DRUG FACTS

Manufacturer: Bath & Body Works, Inc.
Effective date: 2020-11-11
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: legacy-cache
Hydrated at: 2026-08-01 23:01:38

Label at a glance#

ProductAnti-Bacterial Hand Treat Yo Elf Snowkissed Citrus

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

Rub a dime sized drop into hands.

Contacts and useful links#

PhoneLabel contact1-800-395-1001

Websitewww.bathandbodyworks.com

www.bathandbodyworks.com

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 71%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

Decrease bacteria on hands.

WARNINGS

WARNINGS SECTION

For external use only.

When using this product keep out of eyes. Stop use and ask a doctor 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), Fragrance (Parfum), Carbomer, Citrus Aurantium Dulcis (Orange) Peel Oil, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Propylene Glycol, Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Citrus Aurantifolia (Lime) Oil, Retinyl Palmitate, Hydroxypropyl Methylcellulose, Ultramarines (CI 77007), Yellow 5 (CI 19140), Blue 1 (CI 42090), Ext. Violet 2 (CI 60730).

PRODUCT PACKAGING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ABHG Treat Yo Elf Snowkissed Citrus

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Anti-Bacterial Hand Treat Yo Elf Snowkissed Citrus
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62670-5907	62670-5907-0, 62670-5907-1, 62670-5907-3

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
09521aa8-b085-4de7-b7cf-a0c008ebe861			7b7d048d-0f9e-46c2-ae41-9ea6ab792859	2020-11-11	Warnings	Exact identifier spl id: 09521aa8-b085-4de7-b7cf-a0c008ebe861 spl set id: 7b7d048d-0f9e-46c2-ae41-9ea6ab792859

Reported adverse events (FAERS/openFDA)#

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