Label: RASH RELIEF SILVER- dimethicone zinc oxide 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 November 16, 2011

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  • Active Ingredients

    Dimethicone             20%       

    Petrolatum               25%

    Silver                      25 ppm

  • Purpose

    Skin Protectant.

  • Warnings

    - For external use only.

    - When using this product do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.  For external use only. 

    - Stop use and ask a doctor if condition worsens or does not improve in 7 days.


  • Directions

    - Cleanse the skin area thoroughly. 

    - Shake bottle well before use.

    - Spray 4-6 inches from skin using firm/quick trigger motion. No rub-in is required.  Coating slowly dries over time.

    - Reapply 1-3 times per day or as directed by health professional.


  • Inactive Ingredients

    Cyclomethicone, Hexamethyldisiloxane, Lanolin, Light Mineral Oil, Microcrystalline Wax, Protein, Vitamin A Palmitate, Vitamin D3, Water, White Petrolatum

  • INDICATIONS & USAGE

    Manage moisture, friction, and inflammation: skin folds, incontinence dermatitis, venous stasis/pressure ulcers, wounds

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.  If swallowed, get medical help or contact a local poison control center immediately.

  • PRINCIPAL DISPLAY PANEL

    RRSSEnter section text here

  • INGREDIENTS AND APPEARANCE
    RASH RELIEF SILVER  
    dimethicone zinc oxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15071-652
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Dimethicone (UNII: 92RU3N3Y1O) (Dimethicone - UNII:92RU3N3Y1O) Dimethicone20 g  in 100 g
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide25 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    Mineral Oil (UNII: T5L8T28FGP)  
    Cyclomethicone (UNII: NMQ347994Z)  
    Lanolin (UNII: 7EV65EAW6H)  
    Microcrystalline Wax (UNII: XOF597Q3KY)  
    Hexamethyldisiloxane (UNII: D7M4659BPU)  
    Water (UNII: 059QF0KO0R)  
    Cholecalciferol (UNII: 1C6V77QF41)  
    Vitamin A Palmitate (UNII: 1D1K0N0VVC)  
    Petrolatum (UNII: 4T6H12BN9U)  
    Casein (UNII: 48268V50D5)  
    Silver (UNII: 3M4G523W1G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:15071-652-1156 g in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34711/01/2008
    Labeler - Touchless Care Concepts LLC (083459334)
    Registrant - Touchless Care Concepts LLC (083459334)
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