DR. ROTHMANS DERMASHIELD (INSTANT AND LONG LASTING SANITIZER AND MOISTURIZER) SPRAY [HIGH DESERT PHARMACEUTICS, INC.]

DR. ROTHMANS DERMASHIELD (INSTANT AND LONG LASTING SANITIZER AND MOISTURIZER) SPRAY [HIGH DESERT PHARMACEUTICS, INC.]
PDF | XML

NDC 89153-796-04
Set ID 5f8310da-4c22-431f-8fcb-96231f91f594
Category HUMAN OTC DRUG LABEL
Packager High Desert Pharmaceutics, Inc.
Generic Name
Product Class
Product Number
Application Number PART333A
  • ACTIVE INGREDIENT

    Active Ingredients

    • Ethyl Alcohol - 62%
    • Benzalkonium Chloride - 0.10%
  • KEEP OUT OF REACH OF CHILDREN

    Warning

    • Keep out of reach of children.
  • PURPOSE

    Purpose

    • Antiseptic
    • Antibacterial
  • WHEN USING

    Directions

    • Apply by spraying and gently spreading onto skin.
  • WARNINGS

    Warning  

    • For external use only.
    • Flammable keep away from fire or flame
    • Do not use in eyes. In case of contact, rinse eyes thoroughly with water.
  • ASK DOCTOR

    Warning

    • Stop use and ask doctor if irritation and redness persist for more than 72 hours.
  • INDICATIONS & USAGE

    Sanitizer and moisturizer

  • DOSAGE & ADMINISTRATION

    Apply by spraying and gently spreading onto skin

  • INACTIVE INGREDIENT

    Blended Silicone Polyethers

  • PRINCIPAL DISPLAY PANEL

    Dr Rothman's Dermashield

    Image of bottle label

  • INGREDIENTS AND APPEARANCE
    DR. ROTHMANS DERMASHIELD 
    instant and long lasting sanitizer and moisturizer spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:89153-796
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol37.2 g  in 60 g
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride0.06 g  in 60 g
    Inactive Ingredients
    Ingredient NameStrength
    Dimethicone (UNII: 92RU3N3Y1O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:89153-796-0460 g in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2015
    Labeler - High Desert Pharmaceutics, Inc. (830018433)
    Registrant - All Points Manufacturing, LLC (079267697)
    Establishment
    NameAddressID/FEIBusiness Operations
    All Points Manufacturing, LLC079267697manufacture(89153-796)

Related Drugs