FDA.reportPublic FDA data

Ocean Charge APDEO 2.7oz Front Label 1H2026

Manufacturer
Evermark, LLC
Effective date
2026-10-27
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-10-31 01:02:40

Label at a glance#

ProductSuave Mens Invisible Solid Antiperspirant Active Sport
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (18.2%)

OTC - PURPOSE SECTION

Purpose

antiperspirant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings

  • For external use only
  • Do not useon broken skin
  • Ask a doctor before use if you have kidney disease
  • Stop use if rash or irritation occurs
  • Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Fragrance (Parfum), Polyethylene, BHT

DOSAGE & ADMINISTRATION SECTION

Directions apply to underarms only

INDICATIONS & USAGE SECTION

Uses

  • reduces underarm wetness

WARNINGS SECTION

Warnings

  • For external use only
  • Do not use on broken skin
  • Ask a doctor before use if you have kidney disease
  • Stop use if rash or irritation occurs
  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Suave Antiperspirant Active SportSuave Antiperspirant Active Sport

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sauve Antiperspirant Ocean ChargeSauve Antiperspirant Ocean Charge

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Suave Antiperspirant Stress ProtectSuave Antiperspirant Stress Protect

Ocean Charge APDEO 2.7oz Front Label 1H2026

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ocean Charge APDEO 2.7oz Front LabelOcean Charge APDEO 2.7oz Front Label

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83711-12583711-125-27
83711-12683711-126-27
83711-12783711-127-27

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
PPG-14 BUTYL ETHERR199TJT95TIACT
STEARYL ALCOHOL2KR89I4H1YIACT
BHT1P9D0Z171KIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
POLYETHYLENEUG00KM4WR7IACT
FRAGRANCE 135765EM498GW35IACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
PPG-14 BUTYL ETHERR199TJT95TIACT
STEARYL ALCOHOL2KR89I4H1YIACT
BHT1P9D0Z171KIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
POLYETHYLENEUG00KM4WR7IACT
FRAGRANCE 135765EM498GW35IACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
PPG-14 BUTYL ETHERR199TJT95TIACT
STEARYL ALCOHOL2KR89I4H1YIACT
BHT1P9D0Z171KIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
POLYETHYLENEUG00KM4WR7IACT
FRAGRANCE 135765EM498GW35IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42026-03-30full-release2026-06-01 01:52:04

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
4e44211f-5883-36f6-e063-6394a90a173e258aa0ed-7e67-b0fa-e063-6294a90abafe2026-03-30WarningsExact identifier
spl set id: 258aa0ed-7e67-b0fa-e063-6294a90abafe

Reported adverse events (FAERS/openFDA)#

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