Label: RENO CAPS capsule
-
Contains inactivated NDC Code(s)
NDC Code(s): 68151-1928-6 - Packager: Carilion Materials Management
- This is a repackaged label.
- Source NDC Code(s): 63044-622
- Category: HUMAN PRESCRIPTION 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 November 11, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
DESCRIPTION
Reno Caps are black oval softgel imprinted “z622”. These softgels provide water- soluble vitamins.
: Active Ingredients
Each Reno Caps softgel contains:
Vitamin C (Ascorbic Acid)………………………100 mg
Thiamine (as thiamine mononitrate)……………..1.5 mg
Riboflavin………………………………………..1.7 mg
Niacin (as niacinamide)………………………….20 mg
Vitamin B-6 (as pyridoxine Hcl)………………...10 mg
Folate (as folic Acid)…………………………….1 mg
Vitamin B-12 (as cyanocobalam)………………..6 mcg
Biotin……………………………………………..150 mcg
Pantothenic acid (as calcium Pantothenate)……...5 mg
Inactive Ingredients: Gelatin, glycerin, lecithin, soybean oil, yellow beeswax, titanium dioxide, FDC Yellow #6, water, FDC blue #1, FDC Red #40
- INDICATIONS
- PRECAUTIONS
-
DOSAGE AND ADMINISTRATION
One softgel daily, or as directed by a physician. If on dialysis, take after treatment.
Storage: Store at controlled room temperature 15-30C (59-86 F). Keep container tightly closed and protect from heat and moisture.
REN KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILD
Manufactured by :
Catalent Australia PTY LTD
Distributed by:
Nnodum Pharmaceuticals
Cincinnati, Ohio 45240
- RENO CAPS CAPSULE
-
INGREDIENTS AND APPEARANCE
RENO CAPS
reno caps capsuleProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68151-1928(NDC:63044-622) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 100 mg THIAMINE (UNII: X66NSO3N35) (THIAMINE ION - UNII:4ABT0J945J) THIAMINE 1.5 mg RIBOFLAVIN (UNII: TLM2976OFR) (RIBOFLAVIN - UNII:TLM2976OFR) RIBOFLAVIN 1.7 mg NIACIN (UNII: 2679MF687A) (NIACIN - UNII:2679MF687A) NIACIN 20 mg PYRIDOXINE (UNII: KV2JZ1BI6Z) (PYRIDOXINE - UNII:KV2JZ1BI6Z) PYRIDOXINE 10 mg FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8) FOLIC ACID 1 mg BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN 150 ug PANTOTHENIC ACID (UNII: 19F5HK2737) (PANTOTHENIC ACID - UNII:19F5HK2737) PANTOTHENIC ACID 5 mg CYANOCOBALAMIN (UNII: P6YC3EG204) (CYANOCOBALAMIN - UNII:P6YC3EG204) CYANOCOBALAMIN 6 ug Inactive Ingredients Ingredient Name Strength GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) SOYBEAN OIL (UNII: 241ATL177A) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) WATER (UNII: 059QF0KO0R) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) Product Characteristics Color BLACK Score no score Shape OVAL Size 7mm Flavor Imprint Code z622 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68151-1928-6 1 in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 11/30/2008 Labeler - Carilion Materials Management (079239644) Registrant - Carilion Materials Management (079239644) Establishment Name Address ID/FEI Business Operations Carilion Materials Management 079239644 REPACK(68151-1928)