FDA.reportPublic FDA data

BM Potassium dichromate (Kali Dichrom)

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 dichromate (Kali Dichrom)
Active ingredientPOTASSIUM DICHROMATE
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 Dichromate

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 dichromate 6X.jpgPotassium dichromate 6X.jpgEntire package

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeQR CodeM Homoeopathic Pharmaceuticals Expanded cell salt Potassium dichromate 6X (Kali Dichrom 6X) Ref. standard: HPUS DRAP Mfg. Enl. # 0041, Prod. Enl. # 00410122 NDC 82969-1031-1Potassium dichromate 6X.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85816-1031-1BM Potassium dichromate (Kali Dichrom)30000 mg in 1 BOTTLE, GLASSTABLET300002

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85816-103185816-1031-1

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
MAGNESIUM STEARATE70097M6I30IACT
POTASSIUM DICHROMATET4423S18FMACTIB
LACTOSEJ2B2A4N98GIACT

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 dichromate (Kali Dichrom)POTASSIUM DICHROMATEBM Private Limited3803bcb6-74e3-f2fc-e063-6294a90a581f2025-12-02WarningsExact identifier
ndc (package): 85816-1031-1
ndc (product): 85816-1031
ndc11 (package): 85816103101
spl id: 44fb9799-1c7a-b042-e063-6394a90a9aec
spl set id: 3803bcb6-74e3-f2fc-e063-6294a90a581f

Reported adverse events (FAERS/openFDA)#

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