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 
McCord Research

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.

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Viniferamine OTC drug listings

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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

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)

Revised: 1/2022
Document Id: d5ddfab4-3454-7ad8-e053-2a95a90aa720
Set id: 56191aba-7e85-220a-e054-00144ff88e88
Version: 8
Effective Time: 20220118
 
McCord Research