Label: SHEER CONFIDENCE ANTIPERSPIRANT DEODORANT MOONLIT ORCHID (aluminum zirconium tetrachlorohydrex gly- 19% anhydrous stick

  • 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 September 2, 2021

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

View All Sections
  • Active ingredient

    Aluminum zirconium tetrachlorohydrex gly (19% Anhydrous)

  • Purpose

    Antiperspirant

  • INDICATIONS & USAGE

    Use reduces underarm perspiration

  • Warnings

    For external use only

  • DO NOT USE

    Do not use on broken skin

  • ASK DOCTOR

    Ask a dcotor before use if you have kidney disease

  • STOP USE

    Stop use if rash or irritation occurs

  • 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 ■ turn dial to raise product ■ apply to underarms only

  • STORAGE AND HANDLING

    Other information do not freeze or store above 115°F (46°C)

  • Inactive ingredients

    cyclopentasiloxane, stearyl alcohol, C12-15 alkyl benzoate, PPG-14 butyl ether, petrolatum, hydrogenated castor oil, phenyl trimethicone, cetyl alcohol, talc, fragrance, silica, behenyl alcohol, allantoin, aloe barbadensis leaf juice, camella sinensis (green tea) leaf extract, melaleuca alternifolia (tea tree) leaf oil

  • PRINCIPAL DISPLAY PANEL

    AP/DEO label

  • INGREDIENTS AND APPEARANCE
    SHEER CONFIDENCE ANTIPERSPIRANT DEODORANT  MOONLIT ORCHID
    aluminum zirconium tetrachlorohydrex gly (19% anhydrous) stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54473-241
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY19 g  in 57 g
    Inactive Ingredients
    Ingredient NameStrength
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    TALC (UNII: 7SEV7J4R1U)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54473-241-0257 g in 1 APPLICATOR; Type 0: Not a Combination Product01/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35005/01/2013
    Labeler - Melaleuca Inc. (139760102)
    Registrant - Melaleuca Inc. (139760102)
    Establishment
    NameAddressID/FEIBusiness Operations
    KDC/ONE Development Corporation, Inc.204006464manufacture(54473-241)
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!