BM BM38 LIQUID

Manufacturer: BM Private Limited
Effective date: 2026-06-11
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: daily-update
Hydrated at: 2026-06-13 05:10:05

Label at a glance#

ProductBM BM38 DROPS

Active ingredientBERBERIS AQUIFOLIUM ROOT BARK, SULFUR IODIDE, POTASSIUM IODIDE, GRAPHITE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, CENTELLA ASIATICA WHOLE, POTASSIUM BROMIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Berb Aqui 2X (HPUS)
Graphite 18X (HPUS)
Hydrocotyle 2X (HPUS)
Kali Brom 7X (HPUS)
Kali Iodat 7X (HPUS)
Natrum Phos 12X (HPUS)
Sulphur Iodat 7X (HPUS)

INDICATIONS & USAGE SECTION

Indications:
For detail please read the enclosed
package (Product information leaflet).

OTC - PURPOSE SECTION

Indications:
For detail please read the enclosed
package (Product information leaflet).

DOSAGE & ADMINISTRATION SECTION

Dosage:
10-15 drops, 3-4 times a day in
some water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Precautions/storage:
Keep away from children and store
at cool and dry place.

WARNINGS SECTION

Precautions/storage:
Keep away from children and store
at cool and dry place.

INACTIVE INGREDIENT SECTION

Alcohol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 1

bm38

Package 2

bm38 2

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

BM BM38 DROPS
Berb Aqui, Graphite, Hydrocotyle, Kali Brom, Kali Iodat, Natrum Phos, Sulphur Iodat
BERBERIS AQUIFOLIUM ROOT BARK
SULFUR IODIDE
POTASSIUM IODIDE
IODIDE ION
ALCOHOL
GRAPHITE
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
PHOSPHATE ION
CENTELLA ASIATICA WHOLE
POTASSIUM BROMIDE
BROMIDE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85816-2038	85816-2038-1, 85816-2038-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BERBERIS AQUIFOLIUM ROOT BARK	VZJ9F3C3SB	ACTIB
SULFUR IODIDE	L6L8KA2AA0	ACTIB
POTASSIUM IODIDE	1C4QK22F9J	ACTIM
ALCOHOL	3K9958V90M	IACT
GRAPHITE	4QQN74LH4O	ACTIB
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE	70WT22SF4B	ACTIB
CENTELLA ASIATICA WHOLE	7M867G6T1U	ACTIB
POTASSIUM BROMIDE	OSD78555ZM	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 BM38 DROPS	BERB AQUI, GRAPHITE, HYDROCOTYLE, KALI BROM, KALI IODAT, NATRUM PHOS, SULPHUR IODAT	BM Private Limited	53f8163d-28c3-b3b3-e063-6394a90a86da	2026-06-11	Warnings	Exact identifier ndc (package): 85816-2038-2 ndc (package): 85816-2038-1 ndc (product): 85816-2038 ndc11 (package): 85816203802 ndc11 (package): 85816203801 spl id: 53f7fbb4-48a6-bec1-e063-6294a90a3d14 spl set id: 53f8163d-28c3-b3b3-e063-6394a90a86da

Reported adverse events (FAERS/openFDA)#

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