Label: TOTALDRY SENSITIVE WASH- benzethonium chloride spray

  • NDC Code(s): 73703-124-91
  • Packager: Secure Personal Care Products LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 13, 2023

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

View All Sections
  • Active Ingredient

    Benzethonium Chloride 0.12%

  • Purpose

    Antibacterial

  • Uses

    TotalDry™ Sensitive Washis a delicate antibacterial
    formulation for sensitive skin.

  • Warnings

    For external use only.If rash or irritation develops,
    discontinue use. Consult a physician if irritation persists.
    Not for long-term use.

    KEEP OUT OF REACH OF CHILDREN.

  • Directions

    Spray TotalDry™ Sensitive Washliberally on affected
    area, then wipe clean.

  • Ingredients

    Water, Propanediol, Aloe, Barbadensis (Aloe Vera) Leaf Juice,
    Sodium Laureth Sulfate, Disodium Cocoamphodiacetate,
    Polysorbate 80, PEG-12 - PEG-50 Lanolin, Lanolin Alcohol,
    Phenoxyethanol, Ethylhexylglycerin, Citric Acid, Fragrance,
    Yellow 10 (CI 47005)

  • Questions or Comments?

    Please call 1-866-440-0049

  • Label

    Label

  • INGREDIENTS AND APPEARANCE
    TOTALDRY SENSITIVE WASH 
    benzethonium chloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73703-124
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.001212 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    ALOE (UNII: V5VD430YW9)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PPG-12-PEG-50 LANOLIN (UNII: QJP3Q6598J)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73703-124-91237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/01/2020
    Labeler - Secure Personal Care Products LLC (022013246)
    Registrant - Westwood Laboratories LLC (832280635)
    Establishment
    NameAddressID/FEIBusiness Operations
    Westwood Laboratories LLC832280635pack(73703-124) , manufacture(73703-124) , label(73703-124)
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!