Label: ANTIPERSPIRANT DEODORANT ROLL-ON JAFRA DAILY- aluminum chlorohydrate liquid

  • 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 June 22, 2020

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

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredients                         Purpose

    Aluminum Chlorohydrate 12.3%     Antiperspirant

    Uses

    Reduces underarm wetness

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. 

    Stop use if rash or irritation occurs

    Warnings

    For external use only

    Do not use on broken skin

    Ask a doctor before use if you have kidney disease

    apply to underarms only

    Water/Aqua, PEG-40 Stearate, PEG-25 Propylene Glycol Stearate, Stearic Acid, Sorbitan Sesquioleate, Cetyl Alcohol, Magnesium Aluminum Silicate, Fragrance/parfum, DMDM hydantoin, Iodopropynyl Butylcarbamate

  • PRINCIPAL DISPLAY PANEL

    Jafra Daily

    antiperspirant

    deodorant
    roll-on

    60 ml 2 Fl Oz (US)

    antiperspirant carton

  • INGREDIENTS AND APPEARANCE
    ANTIPERSPIRANT DEODORANT ROLL-ON   JAFRA DAILY
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68828-198
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE12.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PEG-40 STEARATE (UNII: ECU18C66Q7)  
    PEG-25 PROPYLENE GLYCOL STEARATE (UNII: X21KPH4633)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68828-198-021 in 1 CARTON08/14/2014
    1NDC:68828-198-0160 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35008/14/2014
    Labeler - Jafra cosmetics International (041676479)
    Registrant - Jafra cosmetics International (041676479)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jafra Manufacturing, S.A. de C.V.814732061manufacture(68828-198)
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!