GILLETTE CLEAR PLUS SCENT BOOST COOL WAVE- aluminum zirconium octachlorohydrex gly gel

Gillette Clear Plus Scent Boost Cool Wave by

Drug Labeling and Warnings

Gillette Clear Plus Scent Boost Cool Wave 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, lactose, microcrystalline cellulose, ferric ammonium ferrocyanide

Questions?

1-800-445-5388

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL

Gillette ®

CLEAR + SCENT BOOST

COOL WAVE

ANTI-WHITE MARK

ANTIPERSPIRANT PROTECTION

ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY

ANTI-PERSPIRANT/DEODORANT

NET WT. 2.85 OZ (80 g)

INGREDIENTS AND APPEARANCE

GILLETTE CLEAR PLUS SCENT BOOST COOL WAVE 
aluminum zirconium octachlorohydrex gly gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-585
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
FERRIC AMMONIUM FERROCYANIDE (UNII: 9R0NVI936I)
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
TETRAHYDROLINALOOL (UNII: UM4XS5M134)
ORANGE TERPENES (UNII: 9J3RG7FX7S)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
ALLYL AMYL GLYCOLATE (UNII: EMX89K493E)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
COUMARIN (UNII: A4VZ22K1WT)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
LINALYL ACETATE (UNII: 5K47SSQ51G)
CITRONELLYL NITRILE, (+/-)- (UNII: GP9AT16H16)
HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)
BENZYL BENZOATE (UNII: N863NB338G)
TETRAHYDROLINALYL ACETATE (UNII: 2NDV3959AX)
DIHYDROMYRCENOL (UNII: 46L1B02ND9)
CITRAL (UNII: T7EU0O9VPP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-585-80	80 g in 1 CYLINDER; Type 0: Not a Combination Product	01/03/2022	11/01/2025
2	NDC: 69423-585-01	2 in 1 CELLO PACK	01/03/2022	11/01/2025
2		80 g in 1 CYLINDER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	01/03/2022	11/01/2025

Labeler - The Procter & Gamble Manufacturing Company (004238200)