Label: SECRET ROLL-ON POWDER FRESH- aluminum chlorohydrate liquid

  • NDC Code(s): 37000-135-22, 37000-135-51, 37000-135-53
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Aluminum chlorohydrate 14% (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, PPG-15 stearyl ether, steareth-2, steareth-20, fragrance, disodium EDTA, BHT

  • Questions?

    1-800-964-1947

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 53 mL Canister Label

    ROLL-ON

    Secret®

    powder fresh

    Aluminum chlorohydrate

    ANTIPERSPIRANT/DEODORANT

    Net Wt. 1.8 FL. OZ. (53 mL)

    Secret1

  • INGREDIENTS AND APPEARANCE
    SECRET ROLL-ON  POWDER FRESH
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-135
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE14 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
    STEARETH-2 (UNII: V56DFE46J5)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-135-2265 mL in 1 CANISTER; Type 0: Not a Combination Product01/21/200109/27/2019
    2NDC:37000-135-5151 mL in 1 CANISTER; Type 0: Not a Combination Product09/27/201711/01/2022
    3NDC:37000-135-5353 mL in 1 CANISTER; Type 0: Not a Combination Product12/07/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01901/21/2001
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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