NDC 15631-2367

Bio-Combination 12

Ferrum Phosphoricum, Kali Phosphoricum, Magnesia Phosphorica, Natrum Muriaticum

Bio-Combination 12 is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Ferrosoferric Phosphate; Potassium Phosphate, Dibasic; Magnesium Phosphate, Dibasic Trihydrate; Sodium Chloride.

Product ID15631-2367_36dea673-c024-40a7-a4f8-3bbdfd2f78da
NDC15631-2367
Product TypeHuman Otc Drug
Proprietary NameBio-Combination 12
Generic NameFerrum Phosphoricum, Kali Phosphoricum, Magnesia Phosphorica, Natrum Muriaticum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-04-11
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameFERROSOFERRIC PHOSPHATE; POTASSIUM PHOSPHATE, DIBASIC; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM CHLORIDE
Active Ingredient Strength12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-2367-7

10000 TABLET in 1 CONTAINER (15631-2367-7)
Marketing Start Date2016-04-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-2367-2 [15631236702]

Bio-Combination 12 TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-11
Inactivation Date2020-01-31

NDC 15631-2367-7 [15631236707]

Bio-Combination 12 TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-11
Inactivation Date2020-01-31

NDC 15631-2367-4 [15631236704]

Bio-Combination 12 TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-11
Inactivation Date2020-01-31

NDC 15631-2367-0 [15631236700]

Bio-Combination 12 TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-11
Inactivation Date2020-01-31

NDC 15631-2367-6 [15631236706]

Bio-Combination 12 TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-11
Inactivation Date2020-01-31

NDC 15631-2367-3 [15631236703]

Bio-Combination 12 TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-11
Inactivation Date2020-01-31

NDC 15631-2367-5 [15631236705]

Bio-Combination 12 TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-11
Inactivation Date2020-01-31

NDC 15631-2367-1 [15631236701]

Bio-Combination 12 TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-11
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FERROSOFERRIC PHOSPHATE12 [hp_X]/1

OpenFDA Data

SPL SET ID:1497c7be-59c6-4125-ae38-1a2c4d4f80d2
Manufacturer
UNII

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