Gillette Clinical

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2022-01-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:11:00

Label at a glance#

ProductGillette Clinical Cool Wave Clear
Active ingredientALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
Label structure10 sections

Dosage and administration

apply to underarms only apply 3 - 4 clicks of product to underarms at bedtime rub in until clear

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum zirconium octachlorohydrex Gly 20% (anhydrous)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED 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
  • apply 3 - 4 clicks of product to underarms at bedtime
  • rub in until clear

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cyclopentasiloxane, dimethicone, propylene glycol, alcohol denat., 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.

PRINCIPAL DISPLAY PANEL - 45 g Canister Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gillette®

CLINICAL

PROTECTION

48 HR

EXTREME

SWEAT PROTECTION

COOL WAVE
CLEAR GEL

ALUMINUM ZIRCONIUM

OCTACHLOROHYDREX GLY
ANTI-PERSPIRANT/DEODORANT

NET WT. 1.6 OZ. (45 g)

GillGill

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
69423-15769423-157-45, 69423-157-73, 69423-157-14

Ingredients#

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

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

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
d6957d5e-ea9c-d1f4-e053-2995a90a5b1241ff7329-e503-1b54-e054-00144ff8d46c2022-01-27WarningsExact identifier
spl id: d6957d5e-ea9c-d1f4-e053-2995a90a5b12
spl set id: 41ff7329-e503-1b54-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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