Label: SECRET HONEYSUCKLE CLEAR- aluminum zirconium octachlorohydrex gly gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated May 21, 2020

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    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
    • apply 2-3 clicks as needed
  • Inactive ingredients

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

  • Questions?

    1-800-964-1947

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 73 g Cylinder Label

    Secret®

    HONEYSUCKLE

    48 HR CLEAR GEL

    ANTIPERSPIRANT

    ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY

    NET WT. 2.6 OZ

    Secret

  • INGREDIENTS AND APPEARANCE
    SECRET HONEYSUCKLE CLEAR 
    aluminum zirconium octachlorohydrex gly gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-434
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY) (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY - UNII:P9D3YP29MY) ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY16 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-434-7373 g in 1 CYLINDER; Type 0: Not a Combination Product01/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35001/15/2020
    Labeler - The Procter & Gamble Manufacturing Company (004238200)