GILLETTE CLEAR PLUS DRI-TECH PACIFIC TIDE- aluminum zirconium octachlorohydrex gly gel

Gillette Clear Plus Dri-Tech Pacific Tide by

Drug Labeling and Warnings

Gillette Clear Plus Dri-Tech Pacific Tide by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Aluminum zirconium octachlorohydrex Gly 17% (anhydrous)

Purpose

Antiperspirant

Use

reduces underarm wetness

Warnings

For external use only.

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irritation occurs

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply to underarms only

Inactive ingredients

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

Questions?

1-800-445-5388

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL

Gillette ®
CLEAR + DRI-TECH

PACIFIC TIDE

ANTI-WHITE MARK

ANTIPERSPIRANT PROTECTION

ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
ANTI-PERSPIRANT/DEODORANT

NET WT. 3.8 OZ (107 g)

INGREDIENTS AND APPEARANCE

GILLETTE CLEAR PLUS DRI-TECH PACIFIC TIDE 
aluminum zirconium octachlorohydrex gly gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-573
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY) (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY - UNII:P9D3YP29MY)	ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY	17 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIMETHICONE (UNII: 92RU3N3Y1O)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-573-10	107 g in 1 CYLINDER; Type 0: Not a Combination Product	06/01/2021	10/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	06/01/2021	10/01/2024

Labeler - The Procter & Gamble Manufacturing Company (004238200)