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
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Contains inactivated NDC Code(s)
NDC Code(s): 71358-011-01, 71358-011-02, 71358-011-03, 71358-011-04, view more71358-012-01, 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 (Box)
- 71358-011-02
- 71358-011-03
- 71358-011-04
- 71358-066-01 (Sachet)
- 71358-066-01 (Box)
- 71358-066-02
- 71358-066-03
- 71358-012-01 (Sachet)
- 71358-012-01 (Box)
- 71358-012-02
- 71358-080-01
- 71358-077-01
- 71358-014-01
- 71358-015-01
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INGREDIENTS AND APPEARANCE
VINIFERAMINE RENEWAL MOISTURIZERÂ
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71358-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 15 mg  in 1 g Inactive Ingredients Ingredient Name Strength ASCORBIC ACID (UNII: PQ6CK8PD0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71358-011-01 144 in 1 BOX 01/23/2014 1 4 g in 1 POUCH; Type 0: Not a Combination Product 2 NDC:71358-011-02 28 g in 1 TUBE; Type 0: Not a Combination Product 01/23/2014 3 NDC:71358-011-03 113 g in 1 TUBE; Type 0: Not a Combination Product 01/23/2014 4 NDC:71358-011-04 907 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 01/23/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/23/2014 VINIFERAMINE SILICONE BARRIERÂ
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71358-066 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 25 mg  in 1 g Inactive Ingredients Ingredient Name Strength ASIATIC ACID (UNII: 9PA5A687X5)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71358-066-01 144 in 1 BOX 01/23/2014 1 4 g in 1 POUCH; Type 0: Not a Combination Product 2 NDC:71358-066-02 113 g in 1 TUBE; Type 0: Not a Combination Product 01/23/2014 3 NDC:71358-066-03 907 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 01/23/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/23/2014 09/30/2019 VINIFERAMINE SKINMINERALZÂ
zinc oxide pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71358-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 125 mg  in 1 g Inactive Ingredients Ingredient Name Strength ASIATIC ACID (UNII: 9PA5A687X5)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71358-012-01 144 in 1 BOX 01/23/2014 1 4 g in 1 POUCH; Type 0: Not a Combination Product 2 NDC:71358-012-02 113 g in 1 TUBE; Type 0: Not a Combination Product 01/23/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/23/2014 VINIFERAMINE HYDROCORTISONE CREAMÂ
hydrocortisone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71358-080 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 10 mg  in 1 g Inactive Ingredients Ingredient Name Strength ASIATIC ACID (UNII: 9PA5A687X5)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71358-080-01 57 g in 1 TUBE; Type 0: Not a Combination Product 01/23/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 01/23/2014 07/31/2017 VINIFERAMINE ANTIFUNGAL CREAMÂ
miconazole nitrate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71358-077 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 20 mg  in 1 g Inactive Ingredients Ingredient Name Strength ASCORBIC ACID (UNII: PQ6CK8PD0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71358-077-01 113 g in 1 TUBE; Type 0: Not a Combination Product 01/23/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 01/23/2014 VINIFERAMINE CLEAN N MOISTÂ
dimethicone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71358-014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 15 mg  in 1 mL Inactive Ingredients Ingredient Name Strength ASIATIC ACID (UNII: 9PA5A687X5)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71358-014-01 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/23/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/23/2014 VINIFERAMINE ANTISEPTIC CLEANSERÂ
benzalkonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71358-015 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.2 mg  in 1 mL Inactive Ingredients Ingredient Name Strength ASIATIC ACID (UNII: 9PA5A687X5)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71358-015-01 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/23/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/23/2014 Labeler - McCord Research (010011284)
