DRUG FACTS

Manufacturer: Bath & Body Works, Inc. | Accel Inc.
Effective date: 2020-12-09
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:35:22

Label at a glance#

ProductAnti-Bacterial Hand Marshmallow Pumpkin Latte

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

INACTIVE INGREDIENTS: Water (Aqua, Eau), Fragrance (Parfum), Carbomer, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Propylene Glycol, Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Hydroxypropyl Methylcellulose, Retinyl Palmitate, Ultramarines (CI 77007), Yellow 5 (CI 19140), Red 40 (CI 16035), Red 33 (CI 17200), Ext. Violet 2 (CI 60730).

PRODUCT PACKAGING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ABHG Marshmallow Pumpkin Latte

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62670-5926-0	2021-07-23	C162847	48780-1	c7ccaba7-2733-fd44-e053-dadaa90aa01b	DRUG FACTS
62670-5926-1	2021-07-23	C162847	48780-1	c7ccaba7-2733-fd44-e053-dadaa90aa01b	DRUG FACTS
62670-5926-3	2021-07-23	C162847	48780-1	c7ccaba7-2733-fd44-e053-dadaa90aa01b	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
62670-5926-0	Anti-Bacterial Hand Marshmallow Pumpkin Latte	29 mL in 1 BOTTLE	GEL	29	4
62670-5926-1	Anti-Bacterial Hand Marshmallow Pumpkin Latte	73 mL in 1 BOTTLE	GEL	73	4
62670-5926-3	Anti-Bacterial Hand Marshmallow Pumpkin Latte	225 mL in 1 BOTTLE, PUMP	GEL	225	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62670-5926	ANTI-BACTERIAL HAND MARSHMALLOW PUMPKIN LATTE (ALCOHOL) GEL [BATH & BODY WORKS, INC.]	4	Legacy NDC, 3 package rows	20201217_5a2d0fb8-94fa-41f8-aaf0-e2011dbef083.zip

Products#

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

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

Anti-Bacterial Hand Marshmallow Pumpkin Latte
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62670-5926	62670-5926-0, 62670-5926-1, 62670-5926-3

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
20b7a24d-c617-41af-8943-0c5f1e666ee8			5a2d0fb8-94fa-41f8-aaf0-e2011dbef083	2020-12-09	Warnings	Exact identifier spl id: 20b7a24d-c617-41af-8943-0c5f1e666ee8 spl set id: 5a2d0fb8-94fa-41f8-aaf0-e2011dbef083

Reported adverse events (FAERS/openFDA)#

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