FDA.reportPublic FDA data

BM Potassium iodide (Kali Iod) 6X

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 02:35:35

Label at a glance#

ProductBM Potassium iodide (Kali Iod) 6X
Active ingredientPOTASSIUM IODIDE
Label structure9 sections

Label contents#

Full prescribing information#

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.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Lactose; MAGNESIUM STEARATE

OTC - ACTIVE INGREDIENT SECTION

Potassium Iodide

INDICATIONS & USAGE SECTION

Uses
See the leaflet enclosed for detail.

OTC - PURPOSE SECTION

Uses
See the leaflet enclosed for detail.

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

Potassium iodide 6X.jpgPotassium iodide 6X.jpgEntire package

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeQR CodeBM Homoeopathic Pharmaceuticals Expanded cell salt Potassium iodide 6X (Kali Iod 6X) Ref. standard: HPUS DRAP Mfg. Enl. # 0041, Prod. Enl. # 000411220362 NDC 82969-1033-1Potassium iodide 6X.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85816-1033-1BM Potassium iodide (Kali Iod) 6X30000 mg in 1 BOTTLE, GLASSTABLET300002

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85816-103385816-1033-1

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
POTASSIUM IODIDE1C4QK22F9JACTIM
LACTOSEJ2B2A4N98GIACT
MAGNESIUM STEARATE70097M6I30IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-06-20full-release2026-06-01 02:34:05

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BM Potassium iodide (Kali Iod) 6XBM POTASSIUM IODIDE (KALI IOD)BM Private Limited3803dd9a-bdec-0a4f-e063-6294a90ada552025-12-02WarningsExact identifier
ndc (package): 85816-1033-1
ndc (product): 85816-1033
ndc11 (package): 85816103301
spl id: 44fbad1f-e864-c63c-e063-6394a90a8b83
spl set id: 3803dd9a-bdec-0a4f-e063-6294a90ada55

Reported adverse events (FAERS/openFDA)#

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