Label: AARICA- aluminum chloride 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 December 19, 2017

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

View All Sections
  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT

    ALUMINUM CHLORIDE HEXAHYDRATE- 15%

  • PURPOSE

    PURPOSE

    ANTIPERSPIRANT

  • INDICATIONS & USAGE

    USES

    REDUCES EXCESSIVE PERSPIRATION AND WETNESS

  • WARNINGS

    WARNING

    For external use only.

  • DO NOT USE

    DO NOT USE ON BROKEN SKIN

  • STOP USE

    STOP USE AND ASK A DOCTOR OR PHARMACIST IF SKIN IRRITATION OR SENSITIVITY DEVELOPS OR INCREASES OR IF THE CONDITION PERSISTS OR GETS WORSE

  • 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 EVENLY AT BEDTIME OR AS DIRECTED BY YOUR DOCTOR.

  • STORAGE AND HANDLING

    OTHER INFORMATION

    STORE AT CONTROLLED ROOM TEMPERATURE.

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS: CAMELLIA SINENSIS (BLACK TEA) LEAF EXTRACT, FRAGRANCE, HYDROXYETHYL CELLULOSE, POLYSORBATE 80, SD 40 ALCOHOL (20%), SODIUM BICARBONATE, WATER

  • QUESTIONS

    QUESTIONS OR SUGGESTIONS? 1.855.763.8733 or visit us at www.thepodiatreecompany.com

  • PRINCIPAL DISPLAY PANEL

    undefined

  • INGREDIENTS AND APPEARANCE
    AARICA 
    aluminum chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54633-413
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE15 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)  
    HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54633-413-0388.72 mL in 1 BOTTLE; Type 0: Not a Combination Product05/06/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35005/06/2014
    Labeler - The Podiatree Company (078656000)
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!