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
Viniferamine Antiseptic Cleanser by
Drug Labeling and Warnings
Viniferamine Antiseptic Cleanser by is a Otc medication manufactured, distributed, or labeled by McCord Research. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
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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
-
INGREDIENTS AND APPEARANCE
VINIFERAMINE RENEWAL MOISTURIZER
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 BARRIER
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 VINIFERAMINE SKINMINERALZ
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 CREAM
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 VINIFERAMINE ANTIFUNGAL CREAM
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 MOIST
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 CLEANSER
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)
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