Label: ULTRAMAX INVISIBLE SOLID - FRESH ANTIPERSPIRANT DEODORANT FRESH- aluminum chlorohydrate stick

  • NDC Code(s): 10237-869-10, 10237-869-26, 10237-869-52
  • Packager: Church & Dwight Co., Inc.
  • 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 December 20, 2022

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

View All Sections
  • ACTIVE INGREDIENT

    Aluminum Chlorohydrate 19%

  • PURPOSE

    Antiperspirant

  • Use

    Use reduces underarm perspiration

  • WARNINGS

    For external use only

  • DO NOT USE

    Do not use on broken skin

  • STOP USE

    Stop use if rash or irritation occurs

  • ASK DOCTOR

    Ask a doctor before use if you have kidney disease

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions Apply a thin layer to underarms only

  • INACTIVE INGREDIENT

    PPG-14 Butyl Ether, Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, Talc, Hydrogenated Castor Oil, Petrolatum, Fragance, Sodium Bicarbonate (Baking Soda), Corn Starch Modified, Polysaccharides, Maltodextrin

  • QUESTIONS

    ? Questions 1-800-248-8820 M-F 9am-5pm ET

  • Principal Display

    REDUCES

    UNDERARM SWEAT

    DUE TO STRESS

    Arm and Hammer
    The Standard of Purity

    ULTRA MAX

    FRESH
    Antiperspirant Deodorant

    SOLID


    NET WT. 1.0 OZ. (28g)

    UMLBF-19122-06_front

  • INGREDIENTS AND APPEARANCE
    ULTRAMAX INVISIBLE SOLID - FRESH  ANTIPERSPIRANT DEODORANT FRESH
    aluminum chlorohydrate stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-869
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE0.19 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    TALC (UNII: 7SEV7J4R1U)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    C12-20 ALKYL BENZOATE (UNII: Y15I6XI14C)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10237-869-2673 g in 1 CANISTER; Type 0: Not a Combination Product02/01/2021
    2NDC:10237-869-1028 g in 1 CANISTER; Type 0: Not a Combination Product02/01/2021
    3NDC:10237-869-52147 g in 1 CANISTER; Type 0: Not a Combination Product02/01/202112/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35002/01/2021
    Labeler - Church & Dwight Co., Inc. (001211952)
    Establishment
    NameAddressID/FEIBusiness Operations
    Church & Dwight Co., Inc.043690812manufacture(10237-869)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!