Gillette Clinical Soft Ultimate Fresh

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2025-12-18
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:26:27

Label at a glance#

ProductGillette Clinical Soft Ultimate Fresh
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure10 sections

Dosage and administration

apply to underarms only apply 3 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 trichlorohydrex Gly 20% (anhydrous)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

  • reduces underarm wetness
  • extra effective

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
  • apply 3 clicks of product to underarms at bedtime
  • rub in until clear

Inactive ingredients

INACTIVE INGREDIENT SECTION

cyclopentasiloxane, dimethicone, tribehenin, petrolatum, cyclodextrin, fragrance, C18-36 acid triglyceride, PPG-14 butyl ether

Questions?

OTC - QUESTIONS SECTION

1-800-445-5388

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 45 g Cylinder Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gillette®
CLINICAL PROTECTION

ULTIMATE FRESH

SOFT SOLID

SOES ON SMOOTH

ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY

ANTIPERSPIRANT/DEODORANT

NET WT. 1.7 OZ (45 g)

GillGill

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69423-256-48Gillette Clinical Soft Ultimate Fresh1 in 1 CARTONCREAM15
69423-256-48Gillette Clinical Soft Ultimate Fresh48 g in 1 CYLINDERCREAM485
69423-256-73Gillette Clinical Soft Ultimate Fresh1 in 1 CARTONCREAM15
69423-256-73Gillette Clinical Soft Ultimate Fresh73 g in 1 CYLINDERCREAM735

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
69423-25669423-256-48, 69423-256-73

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
Gillette Clinical Soft Ultimate FreshALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYThe Procter & Gamble Manufacturing Company5f887376-ebb2-23f6-e053-2a91aa0aff352025-12-18WarningsExact identifier
ndc (package): 69423-256-73
ndc (package): 69423-256-48
ndc (product): 69423-256
ndc11 (package): 69423025673
ndc11 (package): 69423025648
spl id: 463f4eb6-9741-7c2e-e063-6394a90a2a56
spl set id: 5f887376-ebb2-23f6-e053-2a91aa0aff35

Reported adverse events (FAERS/openFDA)#

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