Secret Flawless Clear Clean

Secret Flawless Clear Clean by

Drug Labeling and Warnings

Secret Flawless Clear Clean by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SECRET FLAWLESS CLEAR CLEAN- aluminum zirconium octachlorohydrex gly gel 
The Procter & Gamble Manufacturing Company

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Secret Flawless Clear Clean

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
• apply 2-3 clicks as needed

Inactive ingredients

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

Questions?

1-800-964-1947

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

CRYSTAL CLEAR GEL

SECRET

FLAWLESS CLEAR TM

CLEAN POWDER

CLEAR GEL

ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY

ANTIPERSPIRANT / DEODORANT

NET WT. 2.7 OZ (76 g)

SECRET FLAWLESS CLEAR CLEAN 
aluminum zirconium octachlorohydrex gly gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-734
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
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-734-73	73 g in 1 CYLINDER; Type 0: Not a Combination Product	05/01/2023	10/01/2025
2	NDC: 69423-734-96	96 g in 1 CYLINDER; Type 0: Not a Combination Product	05/01/2023	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	05/01/2023	12/01/2025

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 9/2024

Document Id: 2257244f-65bb-3b63-e063-6394a90aaf3c

34390-5

Set id: 029618f1-1524-08ec-e063-6294a90a0277

Version: 2

Effective Time: 20240917

 

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