FDA.reportPublic FDA data

MC AP DEO Freshwater

Manufacturer
Bath and Body Works, Distr. | SV Labs Corporation
Effective date
2026-06-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-06-11 05:10:25

Label at a glance#

ProductMens Collection Antiperspirant Deodorant Freshwater
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure12 sections

Dosage and administration

apply to underarms only.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Trichlorohydrex GLY 16%

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on broken skin.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease.

OTC - STOP USE SECTION

Stop use if rash or irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply to underarms only.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Dimethicone, Stearyl Alcohol, C15-19 Alkane, Diheptyl Succinate, C12-15 Alkyl Benzoate, Hydrogenated Castor Oil, Cetyl Alcohol, Water (Aqua, Eau), Silica, Aluminum Starch Octenylsuccinate, Fragrance (Parfum), Capryloyl Glycerin/Sebacic Acid Copolymer, Tocopheryl Acetate.

SPL UNCLASSIFIED SECTION

Bath & Body Works, Distr.

95 West Main Street

New Albany, OH 43054

1-800-395-1001

Shop bathandbodyworks.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AP DEO FreshwaterAP DEO Freshwater

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62670-6708-02026-01-29C16284748780-149896155-ae45-586f-e063-e6dba90add90MC AP DEO Freshwater
62670-6708-02026-01-29C16284748780-149896155-ae45-586f-e063-e6dba90add90MC AP DEO Freshwater

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
62670-670862670-6708-0

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
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-07-08full-release2026-06-01 00:14:51

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
Mens Collection Antiperspirant Deodorant FreshwaterALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYBath and Body Works, Distr.1cbd6cc2-41c0-8dca-e063-6394a90a47792026-06-04WarningsExact identifier
ndc (package): 62670-6708-0
ndc (product): 62670-6708
ndc11 (package): 62670670800
spl id: 536e62d2-2022-3b00-e063-6394a90ab599
spl set id: 1cbd6cc2-41c0-8dca-e063-6394a90a4779

Reported adverse events (FAERS/openFDA)#

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