BM Sulphur

Product NDC: 85816-5097
11-digit product format: 858165097
Labeler code: 85816
Product ID: 85816-5097_5c56b3d8-7eec-4919-e063-6294a90a662a
Type: HUMAN OTC DRUG
Nonproprietary name: Sulphur
Dosage form: GLOBULE
Route: ORAL
Labeler: BM Private Limited
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2015-01-01
Substance: SULFUR
Active strength: 30 [hp_C]/1000mg
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: BM Sulphur
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SULFUR	30 [hp_C]/1000mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85816-5097-1	BM Sulphur	30000 mg in 1 BOTTLE, GLASS	GLOBULE	30000		1

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 Sulphur	SULPHUR	BM Private Limited	38e349f3-d65e-b170-e063-6294a90a6512	2025-07-01	Warnings	Exact identifier ndc (product): 85816-5097

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
70FD1KFU70	SULFUR	7704-34-9	SULFUR

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
85816-5097-1	85816509701	30000 mg in 1 BOTTLE, GLASS (85816-5097-1)	30000 mg	2015-01-01	No	No	Current