Label at a glance#

ProductBM Nat Sulph

Active ingredientSODIUM SULFATE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Nat Sulph 6X

INACTIVE INGREDIENT SECTION

Lactose, Magnesium Stearate

INDICATIONS & USAGE SECTION

Helps temporarily relieve: liver discomfort; musculoskeletal discomfort; occasional chest discomfort; water retention; irregular body secretions; headaches; and greenish sputum.

OTC - PURPOSE SECTION

Nat Sulph 6X ...... liver discomfort, water retention, headaches

DOSAGE & ADMINISTRATION SECTION

Use as directed.
Take with water, 3-4 times daily. Ages 12 and older: 5 pellets. Ages 3 to 11: 3 pellets. Ages below 3: consult your doctor.

WARNINGS SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 1 (30g)

NAT SULPH LABEL

NAT SULPH PILLOW BOX

nat sulph carton

Package 2 (500g)

NAT SULPH BIG JAR

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

BM Nat Sulph
Natrum Sulphuricum
LACTOSE
SODIUM SULFATE
SODIUM CATION
MAGNESIUM STEARATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82969-1111	82969-1111-1, 82969-1111-2
85816-1011

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LACTOSE	J2B2A4N98G	IACT
SODIUM SULFATE	0YPR65R21J	ACTIB
MAGNESIUM STEARATE	70097M6I30	IACT

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BM Nat Sulph	NATRUM SULPHURICUM	Total Operations Management LLC DBA:Bestmade Natural Products Micro	53bb2502-509c-ddce-e063-6394a90a04cc	2026-06-08	Warnings	Exact identifier ndc (package): 82969-1111-1 ndc (package): 82969-1111-2 ndc (product): 82969-1111 ndc11 (package): 82969111101 ndc11 (package): 82969111102 spl id: 53bb1234-ba20-00b4-e063-6294a90a0bd7 spl set id: 53bb2502-509c-ddce-e063-6394a90a04cc
BM Nat Sulph	NATRUM SULPHURICUM	BM Private Limited	37b07baf-6d73-91b8-e063-6394a90ab834	2025-12-02	Warnings	Exact identifier ndc (product): 85816-1011

Reported adverse events (FAERS/openFDA)#

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

BMNP Nat Sulph 6X