NDC 0813-9616

O-Cal FA multivitamin

Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine, Folic Acid, Cyanocobalamin, Calcium Carbonate, Ferrous Fumarate, Iodine, Magnesium, Zinc, Copper, And Sodium Fluoride

O-Cal FA multivitamin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Pharmics, Inc.. The primary component is Vitamin A Acetate; Ascorbic Acid; Cholecalciferol; .alpha.-tocopherol Acetate; Thiamine Mononitrate; Riboflavin; Niacin; Pyridoxine; Folic Acid; Cyanocobalamin; Calcium Carbonate; Ferrous Fumarate; Iodine; Magnesium; Zinc; Copper; Sodium Fluoride.

• Product ID: 0813-9616_507a2816-6da4-4b00-af8f-8be0178cb698
• NDC: 0813-9616
• Product Type: Human Prescription Drug
• Proprietary Name: O-Cal FA multivitamin
• Generic Name: Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine, Folic Acid, Cyanocobalamin, Calcium Carbonate, Ferrous Fumarate, Iodine, Magnesium, Zinc, Copper, And Sodium Fluoride
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1970-01-15
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Pharmics, Inc.
• Substance Name: VITAMIN A ACETATE; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACIN; PYRIDOXINE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM CARBONATE; FERROUS FUMARATE; IODINE; MAGNESIUM; ZINC; COPPER; SODIUM FLUORIDE
• Active Ingredient Strength: 2500 [iU]/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1
• Pharm Classes: Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Nicotinic Acid [EPC],Nicotinic Acids [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Copper [CS],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 0813-9616-01

100 TABLET in 1 BOTTLE (0813-9616-01)

• Marketing Start Date: 1970-01-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0813-9616-01 [00813961601]

O-Cal FA multivitamin TABLET

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1970-01-15
• Marketing End Date: 2019-05-31
• Inactivation Date: 2019-11-27
• Reactivation Date: 2020-02-03

Drug Details

Active Ingredients

Ingredient	Strength
VITAMIN A ACETATE	2500 [iU]/1

OpenFDA Data

• SPL SET ID: 3b24458b-6d48-4cc6-8233-81f173277cb8
• Manufacturer:
  • Pharmics, Inc.
• UNII:
  • 1C6V77QF41
  • R5L488RY0Q
  • J41CSQ7QDS
  • PQ6CK8PD0R
  • 9679TC07X4
  • 8ZYQ1474W7
  • 9E8X80D2L0
  • 3LE3D9D6OY
  • 789U1901C5
  • I38ZP9992A
  • TLM2976OFR
  • 2679MF687A
  • 8K0I04919X
  • 935E97BOY8
  • H0G9379FGK
  • KV2JZ1BI6Z
  • P6YC3EG204
• PHarm Class EPC:
  • Vitamin B6 Analog [EPC]
• NUI Code:
  • N0000005657
  • N0000175452
  • N0000192800

Pharmacological Class

• Vitamin A [CS]
• Vitamin A [EPC]
• Vitamin C [EPC]
• Ascorbic Acid [CS]
• Vitamin D [CS]
• Vitamin D [EPC]
• Nicotinic Acid [EPC]
• Nicotinic Acids [CS]
• Vitamin B6 Analog [EPC]
• Vitamin B 6 [Chemical/Ingredient]
• Analogs/Derivatives [Chemical/Ingredient]
• Vitamin B 12 [CS]
• Vitamin B12 [EPC]
• Copper [CS]
• Copper-containing Intrauterine Device [EPC]
• Decreased Embryonic Implantation [PE]
• Decreased Sperm Motility [PE]
• Inhibit Ovum Fertilization [PE]