Bio-Combination 6 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 Chloride; Magnesium Phosphate, Dibasic Trihydrate; Sodium Chloride; Sodium Sulfate.
Product ID | 15631-2361_d8cadba5-2021-4c62-a5c1-c551a432539a |
NDC | 15631-2361 |
Product Type | Human Otc Drug |
Proprietary Name | Bio-Combination 6 |
Generic Name | Ferrum Phosphoricum, Kali Muriaticum, Magnesia Phosphorica, Natrum Muriaticum, Natrum Sulphuricum |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2016-04-11 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc |
Substance Name | FERROSOFERRIC PHOSPHATE; POTASSIUM CHLORIDE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM CHLORIDE; SODIUM SULFATE |
Active Ingredient Strength | 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2016-04-11 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-04-11 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-04-11 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-04-11 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-04-11 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-04-11 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-04-11 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-04-11 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-04-11 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
FERROSOFERRIC PHOSPHATE | 12 [hp_X]/1 |
SPL SET ID: | 0e78544a-1625-4421-9370-aed5bdd1cfa5 |
Manufacturer | |
UNII |