Gillette ® Endurance Cool Wave Clear

Drug Labeling and Warnings

Drug Details [pdf]

GILLETTE ENDURANCE COOL WAVE CLEAR- aluminum zirconium octachlorohydrex gly gel 
The Procter & Gamble Manufacturing Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Gillette ® Endurance Cool Wave Clear

Drug Facts

Active ingredient

Aluminum zirconium octachlorohydrex Gly 16% (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

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

PRINCIPAL DISPLAY PANEL - 107 g Cylinder Label

Gillette®
ENDURANCE

ELIMINATES ODOR
AT THE SOURCE

COOL WAVE
CLEAR GEL

ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
ANTI-PERSPIRANT/DEODORANT

NET WT. 3.8 OZ (107 g)

97150238

GILLETTE ENDURANCE COOL WAVE CLEAR 
aluminum zirconium octachlorohydrex gly gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37000-197
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	16 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: 37000-197-14	14 g in 1 CYLINDER; Type 0: Not a Combination Product	12/20/2014	08/27/2019
2	NDC: 37000-197-80	80 g in 1 CYLINDER; Type 0: Not a Combination Product	12/20/2014	08/27/2019
3	NDC: 37000-197-10	107 g in 1 CYLINDER; Type 0: Not a Combination Product	12/20/2014	08/27/2019
4	NDC: 37000-197-02	2 in 1 CELLO PACK	04/06/2017	08/27/2019
4		80 g in 1 CYLINDER; Type 0: Not a Combination Product
5	NDC: 37000-197-01	2 in 1 CELLO PACK	04/06/2017	08/27/2019
5		107 g in 1 CYLINDER; Type 0: Not a Combination Product
6	NDC: 37000-197-03	3 in 1 CELLO PACK	04/06/2017	08/27/2019
6		107 g in 1 CYLINDER; Type 0: Not a Combination Product
7	NDC: 37000-197-04	5 in 1 CELLO PACK	04/06/2017	08/27/2019
7		107 g in 1 CYLINDER; Type 0: Not a Combination Product
8	NDC: 37000-197-05	6 in 1 CELLO PACK	04/06/2017	08/27/2019
8		107 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 final	part350	12/20/2014	08/27/2019

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Establishment
Name	Address	ID/FEI	Business Operations
Procter and Gamble Manufacturing Co.		017745779	manufacture(37000-197)

Revised: 12/2017

Document Id: 60a19879-c0bf-3c6f-e053-2991aa0adfe0

34390-5

Set id: 8bd1fd92-1c4c-485a-b80a-65a2eb973ef7

Version: 5

Effective Time: 20171218

 

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