Label: VITA-15 injection
- NDC Code(s): 59051-8882-5
- Packager: Neogen Corporation
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 12, 2019
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- Official Label (Printer Friendly)
- Indications:
-
Each mL contains:
Pyridoxine HCl ...................................................... 10 mg
Riboflavin 5'-PO4-Na•2H2O USP .............................. 10 mg
d-Panthenol ......................................................... 15 mg
Niacinamide ....................................................... 100 mg
Inositol ............................................................... 10 mg
Choline Chloride ................................................... 10 mg
Biotin .................................................................. 10 mcg
L-Lysine HCl ......................................................... 20 mg
Glycine ................................................................ 20 mg
Cobalt Gluconate 8 H2O ......................................... 0.7 mg
Benzyl Alcohol ........................................................... 2%
Water for Injection .................................................... q.s. - Dosage & Administration:
- CAUTION:
- AVOID EXPOSURE TO LIGHT Store at refrigerated temperatures between 2° and 8°C (36° -46°F).
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VITA-15
vita-15 injectionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:59051-8882 Route of Administration INTRAMUSCULAR, INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) (PYRIDOXINE - UNII:KV2JZ1BI6Z) PYRIDOXINE HYDROCHLORIDE 10 mg in 1 mL RIBOFLAVIN 5'-PHOSPHATE SODIUM (UNII: 20RD1DZH99) (FLAVIN MONONUCLEOTIDE - UNII:7N464URE7E) FLAVIN MONONUCLEOTIDE 10 mg in 1 mL DEXPANTHENOL (UNII: 1O6C93RI7Z) (DEXPANTHENOL - UNII:1O6C93RI7Z) DEXPANTHENOL 15 mg in 1 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 100 mg in 1 mL INOSITOL (UNII: 4L6452S749) (INOSITOL - UNII:4L6452S749) INOSITOL 10 mg in 1 mL CHOLINE CHLORIDE (UNII: 45I14D8O27) (CHOLINE - UNII:N91BDP6H0X) CHOLINE CHLORIDE 10 mg in 1 mL BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN 10 ug in 1 mL LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM) (LYSINE - UNII:K3Z4F929H6) LYSINE 20 mg in 1 mL GLYCINE (UNII: TE7660XO1C) (GLYCINE - UNII:TE7660XO1C) GLYCINE 20 mg in 1 mL COBALTOUS GLUCONATE (UNII: 26SK597UWV) (COBALTOUS CATION - UNII:AI1MR454XG) COBALTOUS GLUCONATE 0.7 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) 20 mg in 1 mL WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59051-8882-5 100 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/22/2011 Labeler - Neogen Corporation (042125879) Registrant - Nova-Tech, Inc (196078976) Establishment Name Address ID/FEI Business Operations Nova-Tech, Inc 196078976 manufacture