BM FERR PHOS 6X HOMEOPATHIC POTENCY

Manufacturer: BM Private Limited
Effective date: 2026-05-31
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: daily-update
Hydrated at: 2026-06-03 18:04:04

Label at a glance#

ProductBM FERR PHOS POTENCY

Active ingredientFERROSOFERRIC PHOSPHATE

Label structure8 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

In-Active ingredient:
Vehicle used as in-Active ethanol 90–95% v/v.

INDICATIONS & USAGE SECTION

Indications:
As per recognized Homoeopathic Pharmacopoeia and Materia Medica.

OTC - PURPOSE SECTION

Indications:
As per recognized Homoeopathic Pharmacopoeia and Materia Medica.

DOSAGE & ADMINISTRATION SECTION

For oral use only

OTC - ACTIVE INGREDIENT SECTION

Ferr Phos 6X

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

Warnings/Precautions:

For oral use only. Contains ethanol.
Handle with care. Please read on the outer carton.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ferr phos

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

BM FERR PHOS POTENCY
Ferr Phos
ALCOHOL
FERROSOFERRIC PHOSPHATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85816-6033	85816-6033-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
FERROSOFERRIC PHOSPHATE	91GQH8I5F7	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BM FERR PHOS POTENCY	FERR PHOS	BM Private Limited	53236607-b905-33f7-e063-6394a90a9965	2026-05-31	Warnings	Exact identifier ndc (package): 85816-6033-1 ndc (product): 85816-6033 ndc11 (package): 85816603301 spl id: 53236607-b906-33f7-e063-6394a90a9965 spl set id: 53236607-b905-33f7-e063-6394a90a9965

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.