FDA.reportPublic FDA data

Gillette Clear Ocean Blast

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2022-06-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:58:14

Label at a glance#

ProductGillette Clear Ocean Blast
Active ingredientALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
Label structure10 sections

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum zirconium octachlorohydrex Gly 16% (anhydrous)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

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

water, alcohol denat., cyclopentasiloxane, propylene glycol, dimethicone, calcium chloride, PEG/PPG-18/18 dimethicone, fragrance

Questions?

OTC - QUESTIONS SECTION

1-800-445-5388

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gillette ®

CLEAR GEL

Scent Xtend Technology+


OCEAN BLAST

ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY

ANTI-PERSPIRANT/DEODORANT

NET WT. 3.8 OZ (107 g)

GilletteGillette

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69423-239-102022-06-23C16284748780-1d6a99b39-6cf0-a426-e053-dadaa90af4c2Gillette ® Clear Ocean Blast
69423-239-102022-01-28C16284748780-1d6a99b39-6cf0-a426-e053-dadaa90af4c2Gillette ® Clear Ocean Blast

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-23969423-239-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
CYCLOMETHICONE 50THT5PCI0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DIMETHICONE92RU3N3Y1OIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLYP9D3YP29MYACTIB

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
e2224f17-524b-2eac-e053-2a95a90a22c25bc445f3-6fc1-757f-e053-2991aa0a77012022-06-23WarningsExact identifier
spl id: e2224f17-524b-2eac-e053-2a95a90a22c2
spl set id: 5bc445f3-6fc1-757f-e053-2991aa0a7701

Reported adverse events (FAERS/openFDA)#

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