Label: VINIFERAMINE RENEWAL MOISTURIZER- dimethicone cream
VINIFERAMINE SILICONE BARRIER- dimethicone cream
VINIFERAMINE SKINMINERALZ- zinc oxide paste
VINIFERAMINE HYDROCORTISONE CREAM- hydrocortisone cream
VINIFERAMINE ANTIFUNGAL CREAM- miconazole nitrate cream
VINIFERAMINE CLEAN N MOIST- dimethicone lotion
VINIFERAMINE ANTISEPTIC CLEANSER- benzalkonium chloride spray

  • NDC Code(s): 71358-011-01, 71358-011-02, 71358-011-03, 71358-011-04, view more
    71358-012-01, 71358-012-02, 71358-014-01, 71358-015-01, 71358-066-01, 71358-066-02, 71358-066-03, 71358-077-01, 71358-080-01
  • Packager: McCord Research
  • 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 January 18, 2022

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  • 71358-011-01 (Sachet)

    71358-011-01 (Sachet)

  • 71358-011-01 (Box)

    ​71358-011-01 (Box)

  • 71358-011-02

    71358-011-02

  • 71358-011-03

    71358-011-03

  • 71358-011-04

    71358-011-04

  • 71358-066-01 (Sachet)

    71358-066-01 (Sachet)

  • 71358-066-01 (Box)

    ​71358-066-01 (Box)

  • 71358-066-02

    71358-066-02

  • 71358-066-03

    71358-066-03

  • 71358-012-01 (Sachet)

    71358-012-01 (Sachet)

  • 71358-012-01 (Box)

    ​71358-012-01 (Box)

  • 71358-012-02

    71358-012-02

  • 71358-080-01

    71358-080-01

  • 71358-077-01

    71358-077-01

  • 71358-014-01

    71358-014-01

  • 71358-015-01

    71358-015-01

  • INGREDIENTS AND APPEARANCE
    VINIFERAMINE RENEWAL MOISTURIZER 
    dimethicone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71358-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE15 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71358-011-01144 in 1 BOX01/23/2014
    14 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:71358-011-0228 g in 1 TUBE; Type 0: Not a Combination Product01/23/2014
    3NDC:71358-011-03113 g in 1 TUBE; Type 0: Not a Combination Product01/23/2014
    4NDC:71358-011-04907 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/23/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34701/23/2014
    VINIFERAMINE SILICONE BARRIER 
    dimethicone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71358-066
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE25 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ASIATIC ACID (UNII: 9PA5A687X5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71358-066-01144 in 1 BOX01/23/2014
    14 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:71358-066-02113 g in 1 TUBE; Type 0: Not a Combination Product01/23/2014
    3NDC:71358-066-03907 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/23/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34701/23/201409/30/2019
    VINIFERAMINE SKINMINERALZ 
    zinc oxide paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71358-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE125 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ASIATIC ACID (UNII: 9PA5A687X5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71358-012-01144 in 1 BOX01/23/2014
    14 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:71358-012-02113 g in 1 TUBE; Type 0: Not a Combination Product01/23/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34701/23/2014
    VINIFERAMINE HYDROCORTISONE CREAM 
    hydrocortisone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71358-080
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ASIATIC ACID (UNII: 9PA5A687X5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71358-080-0157 g in 1 TUBE; Type 0: Not a Combination Product01/23/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34801/23/201407/31/2017
    VINIFERAMINE ANTIFUNGAL CREAM 
    miconazole nitrate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71358-077
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71358-077-01113 g in 1 TUBE; Type 0: Not a Combination Product01/23/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333C01/23/2014
    VINIFERAMINE CLEAN N MOIST 
    dimethicone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71358-014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE15 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ASIATIC ACID (UNII: 9PA5A687X5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71358-014-01236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/23/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34701/23/2014
    VINIFERAMINE ANTISEPTIC CLEANSER 
    benzalkonium chloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71358-015
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ASIATIC ACID (UNII: 9PA5A687X5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71358-015-01236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/23/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/23/2014
    Labeler - McCord Research (010011284)