BM Calc Sulph

Manufacturer
BM Private Limited
Effective date
2025-12-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:35:31

Label at a glance#

ProductBM Calc Sulph
Active ingredientCALCIUM SULFATE ANHYDROUS
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Calcium Sulphuricum

INACTIVE INGREDIENT SECTION

Lactose; MAGNESIUM STEARATE

DOSAGE & ADMINISTRATION SECTION

Directions:
Adult: Four tablets three times a day.
Ages below 12: half of the same or as prescribed by a homeopathic physician.

CONTRAINDICATIONS SECTION

Contra-indications:
Traditional biochemic remedy do not interact with other remedies, herbs, or other supplements.

WARNINGS SECTION

Warnings and Storage:

Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings and Storage:

Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.

INDICATIONS & USAGE SECTION

Uses
See the leaflet enclosed for detail.

OTC - PURPOSE SECTION

Uses
See the leaflet enclosed for detail.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package 1 (30g)

calc sulphcalc sulph

package 2 (500g)

calc sulph 6xcalc sulph 6x

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeQR Code BM Homoeopathic Pharmaceuticals BM's Calcium sulphuricum 6X (Calc sulph 6X) Ref. standard: GHP/HAB (Lactose base) DRAP Mfg. Enl. # 0041, Prod. Enl. # 0041.0636 NDC 82969-1003-1Calc Sulph.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85816-1003-1BM Calc Sulph30000 mg in 1 BOTTLE, GLASSTABLET300002
85816-1003-2BM Calc Sulph500000 mg in 1 JARTABLET5000002

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85816-100385816-1003-1, 85816-1003-2

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Biochemic Tissue Salt KitCELL SALTSBM Private Limited450e1d26-c1a8-dd79-e063-6394a90aa0e62025-12-03WarningsExact identifier
ndc (package): 85816-1003-1
ndc11 (package): 85816100301
BM Calc SulphCALCAREA SULPHURICABM Private Limited37b02adb-6cd4-636b-e063-6394a90aa17a2025-12-02WarningsExact identifier
ndc (package): 85816-1003-1
ndc (package): 85816-1003-2
ndc (product): 85816-1003
ndc11 (package): 85816100302
ndc11 (package): 85816100301
spl id: 44f99ded-08ba-814b-e063-6294a90ac908
spl set id: 37b02adb-6cd4-636b-e063-6394a90aa17a

Reported adverse events (FAERS/openFDA)#

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