FDA.reportPublic FDA data

DRUG FACTS

Manufacturer
Bath & Body Works, Inc.
Effective date
2020-12-14
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 Eucalyptus Tea
Active ingredientALCOHOL
Label structure10 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

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, Lactose, Eucalyptus Globulus Leaf Oil, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Propylene Glycol, Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Camellia Sinensis Leaf Extract, Retinyl Palmitate, Hydroxypropyl Methylcellulose, Ultramarines (CI 77007), 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 Eucalyptus TeaABHG Eucalyptus Tea

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62670-5979-02022-01-28C16284748780-1c7ccaba7-11ac-fd44-e053-dadaa90aa01bDRUG FACTS
62670-5979-12022-01-28C16284748780-1c7ccaba7-11ac-fd44-e053-dadaa90aa01bDRUG FACTS
62670-5979-32022-01-28C16284748780-1c7ccaba7-11ac-fd44-e053-dadaa90aa01bDRUG FACTS
62670-5979-02021-11-14C16284748780-1c7ccaba7-11ac-fd44-e053-dadaa90aa01bDRUG FACTS
62670-5979-12021-11-14C16284748780-1c7ccaba7-11ac-fd44-e053-dadaa90aa01bDRUG FACTS
62670-5979-32021-11-14C16284748780-1c7ccaba7-11ac-fd44-e053-dadaa90aa01bDRUG FACTS
62670-5979-02021-07-23C16284748780-1c7ccaba7-11ac-fd44-e053-dadaa90aa01bDRUG FACTS
62670-5979-12021-07-23C16284748780-1c7ccaba7-11ac-fd44-e053-dadaa90aa01bDRUG FACTS
62670-5979-32021-07-23C16284748780-1c7ccaba7-11ac-fd44-e053-dadaa90aa01bDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62670-5979-0Anti-Bacterial Hand Eucalyptus Tea29 mL in 1 BOTTLEGEL294
62670-5979-1Anti-Bacterial Hand Eucalyptus Tea73 mL in 1 BOTTLEGEL734
62670-5979-3Anti-Bacterial Hand Eucalyptus Tea236 mL in 1 BOTTLE, PUMPGEL2364

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62670-5979ANTI-BACTERIAL HAND EUCALYPTUS TEA (ALCOHOL) GEL [BATH & BODY WORKS, INC.]4Legacy NDC, 3 package rows20201217_741010a7-3f05-43eb-ba59-9c8de073d1b0.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
62670-597962670-5979-0, 62670-5979-1, 62670-5979-3

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
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
5101ccab-bb9d-401b-9f3c-95db188e65e6741010a7-3f05-43eb-ba59-9c8de073d1b02020-12-14WarningsExact identifier
spl id: 5101ccab-bb9d-401b-9f3c-95db188e65e6
spl set id: 741010a7-3f05-43eb-ba59-9c8de073d1b0

Reported adverse events (FAERS/openFDA)#

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