FDA.reportPublic FDA data

Gillette Clear Plus Dri-Tech Wild Rain

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2024-01-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:16:02

Label at a glance#

ProductGillette Clear Plus Dri-Tech Wild Rain
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 17% (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 + DRI-TECH

Wiild Rain

ANTI-WHITE MARK

ANTIPERSPIRANT PROTECTION

ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY

ANTI-PERSPIRANT/DEODORANT

NET WT. 3.8 OZ (107 g)

GilGil

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-58169423-581-10, 69423-581-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
LIMONENE, (+)-GFD7C86Q1WIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
CYCLOMETHICONE 50THT5PCI0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DIMETHICONE92RU3N3Y1OIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLYP9D3YP29MYACTIB
2-TERT-BUTYLCYCLOHEXYL ACETATE, CIS-87JN7005XUIACT
2-ETHYL-4-(2,2,3-TRIMETHYLCYCLOPENT-3-EN-1-YL)BUT-2-EN-1-OLV1IKN2SI96IACT
TETRAHYDROLINALOOLUM4XS5M134IACT
CEDRAMBER84S7T555CVIACT
ORANGE OILAKN3KSD11BIACT
2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OLVK5ZHH2T3FIACT
DIPROPYLENE GLYCOLE107L85C40IACT
HEXAMETHYLINDANOPYRAN14170060ATIACT
TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES2JU6ZH6GREIACT
DIHYDROMYRCENOL46L1B02ND9IACT

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
0e24e82c-aa04-839b-e063-6394a90a6d59e21f34ae-e880-493c-e053-2a95a90ade832024-01-04WarningsExact identifier
spl id: 0e24e82c-aa04-839b-e063-6394a90a6d59
spl set id: e21f34ae-e880-493c-e053-2a95a90ade83

Reported adverse events (FAERS/openFDA)#

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