Label: AXE- acne control body hand and face bar soap

  • 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 April 29, 2022

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  • AXE ACNE CONTROL BODY, HAND AND FACE BAR - Salicylic Acid

    Dove Care & Protect Antibacterial Beauty Bar

  • Drug Facts

    Active ingredient

    Salicylic Acid (2.0)

  • Purpose

    Acne Treatment

  • Uses

    For the treatment of acne

  • Warnings

    • For external use only
    • When using this product, skin irritation and dryness is more likely to occur if you use anoter tropical acne medication at the same time. If irritation occurs, only use one tropical acne medication at a time.

  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children except under adult supervision.

    If swallowed, get medical help or contact a poison control Center right away.

  • Directions

    Lather on body and face. Rinse. Feel great.

  • Inactive ingredients

    Sodium Palmate, Sodium Palm Kernelate, Water (Aqua), Glycerin, Sodium Gluconate, Fragrance (Parfum), Palm Acid, Sodium Chloride, Palm Kernel Acid, Petroselinum Sativum (Parsley) Leaf Powder, Curcuma Longa (Tumeric) Root Extract, Melaleuca Alternifolia (Ta Tree) Flower/Leaf/Stem Extract, Titanium Dioxide (CI 77891), Ext. Yellow 7 (CI 42053), Iron Oxides (CI 77499).

  • Question/Comments?

    1-800-450-7580

  • Packaging

    Axe Acne Control Bar

  • INGREDIENTS AND APPEARANCE
    AXE 
    acne control body hand and face bar soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2025
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    EXT. D&C YELLOW NO. 7 (UNII: 08F8S9O3I5)  
    SODIUM PALMATE (UNII: S0A6004K3Z)  
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    PALM ACID (UNII: B6G0Y5Z616)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    PALM KERNEL ACID (UNII: 79P21R4317)  
    PARSLEY (UNII: 58FMD0Q0EV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2025-1127.5 g in 1 CARTON; Type 0: Not a Combination Product04/29/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D04/29/2022
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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