Label: CA-REZZ NORISC ANTIBACTERIAL SKIN CARE- benzethonium chloride cream

  • NDC Code(s): 60762-112-04, 60762-112-09
  • Packager: FNC MEDICAL CORPORATION
  • Category: HUMAN OTC DRUG LABEL

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 October 3, 2023

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  • ACTIVE INGREDIENT

    BENZETHONIUM CHLORIDE 0.2%

  • PURPOSE

    ANTIBACTERIAL

  • USES

    CA-REZZ NORSIC CREAM IS A NON-GREASY ANTIBACTERIAL CREAM SPECIALLY FORMULATED TO SOOTHE SKIN TISSUE. IT IS IDEAL FOR USE ON IRRITATED SKIN. IT REDUCES COMMON GERMS THAT CAN CAUSE PAINFUL RASHES.

  • WARNINGS

    FOR EXTERNAL USE ONLY. IF RASH OR IRRITATION DEVELOP, DISCONTINUE USE. CONSULT A PHYSICIAN IF IRRITATION PERSISTS.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • DIRECTIONS

    1. APPLY A SMALL AMOUNT OF CREAM TO SKIN AND RUB GENTLY.
    2. USE AS A MASSAGE CREAM FOR IMMOBILE PATIENTS TO IMPROVE CIRCULATION.

  • OTHER INFORMATION

    CA-REZZ NORSIC CREAM IS ENRICHED WITH VITAMINS A, D & E, ALOE VERA AND ALLANTOIN.

  • INACTIVE INGREDIENTS

    DEIONIZED WATER, MINERAL OIL, ALOE VERA EXTRACT, PROPYLENE GLYCOL, STEARIC ACID, GLYCERYL STEARATE AND PEG 100 STEARATE, SAFFLOWER OIL, CETYL ALCOHOL, TRIETHANOLAMINE, SORBITAN, ISOSTEARATE, DIMETHICONE, ALLANTOIN, TOCOPHERYL ACETATE, RETINYL PALMITATE, ERGOCALCIFEROL, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN, FRAGRANCE.

  • QUESTIONS/COMMENTS?

    PLEASE CALL (800) 440-2888

  • PRINCIPAL DISPLAY PANEL

    Antibacterial Skin Care_Norisc Cream_120g_LBL

    Antibacterial Skin Care_Norisc Cream_275g_LBL

  • INGREDIENTS AND APPEARANCE
    CA-REZZ NORISC   ANTIBACTERIAL SKIN CARE
    benzethonium chloride cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60762-112
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    ALOE VERA WHOLE (UNII: KIZ4X2EHYX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ALLANTOIN (UNII: 344S277G0Z)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    ERGOCALCIFEROL (UNII: VS041H42XC)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60762-112-09275 g in 1 TUBE; Type 0: Not a Combination Product02/05/2018
    2NDC:60762-112-04120 g in 1 TUBE; Type 0: Not a Combination Product02/05/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/05/2018
    Labeler - FNC MEDICAL CORPORATION (849207519)
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