NDC 0642-0092

Vitafol Plus

Omega-3 Fatty Acids, Niacin, .alpha.-tocopherol, Vitamin D, Lauric Acid, Vitamin A, Ascorbic Acid, Thiamine Mononitrate, Riboflavin, Pyridoxine Hydrochloride, Cyanocobalamin, Iron, Zinc, Copper, Iodine, Magnesium, And Folic Acid

Vitafol Plus is a Oral Capsule, Liquid Filled in the Human Prescription Drug category. It is labeled and distributed by Everett Laboratories, Inc.. The primary component is Omega-3 Fatty Acids; Niacin; .alpha.-tocopherol; Vitamin D; Lauric Acid; Vitamin A; Ascorbic Acid; Thiamine Mononitrate; Riboflavin; Pyridoxine Hydrochloride; Cyanocobalamin; Iron; Zinc; Copper; Iodine; Magnesium; Folic Acid.

• Product ID: 0642-0092_bb1edb09-09b6-48dc-9acb-1592639035e6
• NDC: 0642-0092
• Product Type: Human Prescription Drug
• Proprietary Name: Vitafol Plus
• Generic Name: Omega-3 Fatty Acids, Niacin, .alpha.-tocopherol, Vitamin D, Lauric Acid, Vitamin A, Ascorbic Acid, Thiamine Mononitrate, Riboflavin, Pyridoxine Hydrochloride, Cyanocobalamin, Iron, Zinc, Copper, Iodine, Magnesium, And Folic Acid
• Dosage Form: Capsule, Liquid Filled
• Route of Administration: ORAL
• Marketing Start Date: 2012-04-23
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Everett Laboratories, Inc.
• Substance Name: OMEGA-3 FATTY ACIDS; NIACIN; .ALPHA.-TOCOPHEROL; VITAMIN D; LAURIC ACID; VITAMIN A; ASCORBIC ACID; THIAMINE MONONITRATE; RIBOFLAVIN; PYRIDOXINE HYDROCHLORIDE; CYANOCOBALAMIN; IRON; ZINC; COPPER; IODINE; MAGNESIUM; FOLIC ACID
• Active Ingredient Strength: 200 mg/1; mg/1; [iU]/1; [iU]/1; mg/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1
• Pharm Classes: Vitamin D [CS],Vitamin D [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 0642-0092-30

5 BLISTER PACK in 1 BOX (0642-0092-30) > 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

• Marketing Start Date: 2012-04-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0642-0092-01 [00642009201]

Vitafol Plus CAPSULE, LIQUID FILLED

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-04-23
• Inactivation Date: 2020-01-31

NDC 0642-0092-30 [00642009230]

Vitafol Plus CAPSULE, LIQUID FILLED

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-04-23
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
OMEGA-3 FATTY ACIDS	200 mg/1

OpenFDA Data

• SPL SET ID: 3af5077a-54ee-41de-8750-dce3eea327e6
• Manufacturer:
  • Everett Laboratories, Inc.
• UNII:
  • I38ZP9992A
  • 68Y4CF58BV
  • 1160N9NU9U
  • 71M78END5S
  • J41CSQ7QDS
  • 2679MF687A
  • 9679TC07X4
  • E1UOL152H7
  • 9VU1KI44GP
  • 789U1901C5
  • TLM2976OFR
  • PQ6CK8PD0R
  • 8K0I04919X
  • 935E97BOY8
  • H4N855PNZ1
  • 81G40H8B0T
  • P6YC3EG204

Pharmacological Class

• Vitamin D [CS]
• Vitamin D [EPC]
• Vitamin C [EPC]
• Ascorbic Acid [CS]
• Vitamin B6 Analog [EPC]
• Vitamin B 6 [Chemical/Ingredient]
• Analogs/Derivatives [Chemical/Ingredient]
• Vitamin B 12 [CS]
• Vitamin B12 [EPC]