FDA.reportPublic FDA data

BM Nat Phos

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 02:35:32

Label at a glance#

ProductBM Nat Phos
Active ingredientSODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Natrum Phosphoricum

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Lactose, Magnesium Stearate

INDICATIONS & USAGE SECTION

Uses
See the leaflet enclosed for detail.

OTC - PURPOSE SECTION

Uses
See the leaflet enclosed for detail.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 1 (30g)

Nat PhosNat Phos

Package 2 (500g)

nat phos 6xnat phos 6x

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeQR CodeBM Homoeopathic Pharmaceuticals BM's Natrium phosphoricum 6X (Nat phos 6X) Ref. standard: GHP/HAB (Lactose base) DRAP Mfg. Enl. # 0041, Prod. Enl. # 0041.0643 NDC 82969-1010-1 Nat Phos.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85816-1010-1BM Nat Phos30000 mg in 1 BOTTLE, GLASSTABLET300002
85816-1010-2BM Nat Phos500000 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
85816-101085816-1010-1, 85816-1010-2

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
NameUNIIKind
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE70WT22SF4BACTIB
LACTOSEJ2B2A4N98GIACT
MAGNESIUM STEARATE70097M6I30IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-06-16full-release2026-06-01 02:34:01

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): 85816-1010-1
ndc11 (package): 85816101001
BM Nat PhosNATRUM PHOSPHORICUMBM Private Limited37b0db27-eede-9141-e063-6294a90a8a0c2025-12-02WarningsExact identifier
ndc (package): 85816-1010-1
ndc (package): 85816-1010-2
ndc (product): 85816-1010
ndc11 (package): 85816101002
ndc11 (package): 85816101001
spl id: 44fa41af-1b39-208c-e063-6394a90a3bbe
spl set id: 37b0db27-eede-9141-e063-6294a90a8a0c

Reported adverse events (FAERS/openFDA)#

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