FDA.reportPublic FDA data

Gillette

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-06-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-07-17 21:36:09

Label at a glance#

ProductGillette Clinical Protection Arctic Ice Soft
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, tribehenin, dimethicone, 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 - 73 g Cylinder Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gillette®
CLINICAL PROTECTION

ARCTIC ICE

SOFT SOLID

ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY

ANTIPERSPIRANT/DEODORANT

NET WT. 2.6 OZ (73 g)

GILGIL

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix21376416GIL.jpg

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
84126-01984126-019-48, 84126-019-73

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
BETADEXJV039JZZ3AIACT
C18-36 ACID TRIGLYCERIDEZRA72DR3R7IACT
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE92RU3N3Y1OIACT
PETROLATUM4T6H12BN9UIACT
TRIBEHENIN8OC9U7TQZ0IACT
PPG-14 BUTYL ETHERR199TJT95TIACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-12-31full-release2026-06-01 01:29:53

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 Protection Arctic Ice SoftALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYThe Procter & Gamble Manufacturing Company2048e36d-71fe-3831-e063-6394a90a55e52026-06-24WarningsExact identifier
ndc (package): 84126-019-48
ndc (package): 84126-019-73
ndc (product): 84126-019
ndc11 (package): 84126001948
ndc11 (package): 84126001973
spl id: 5502122a-7824-7d77-e063-6294a90aa0b2
spl set id: 2048e36d-71fe-3831-e063-6394a90a55e5

Reported adverse events (FAERS/openFDA)#

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