KALI BICHROMICUM

Manufacturer: Remedy Makers
Effective date: 2010-03-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:02:14

Label at a glance#

ProductKALI BICHROMICUM

Active ingredientPOTASSIUM DICHROMATE

Label structure2 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Free from yeast, wheat, corn, and soy.
DIRECTIONS: Dissolve 3 or 4 pellets
in mouth or under tongue 3 times a day or as directed by a physician.
Children 2 years and older take 1/2
adult dose.
INDICATIONS: To be used according
to standard homeopathic indications
for self limiting conditions such as
those indicated on the front panel or as directed by a physician.
Warnings: *Use only if cap and
seal are unbroken. * Keep this and all medications out of reach of children.
* If symptoms persist for more then 3
days, consult your physician.
*As with any drug, if your are pregnant or nursing a baby, seek the advice of a
health professional before using this product.*Store tightly closed in a cool, dark place.
Made according to The Homeopathic Pharmacopoeia of the United States by: Remedy Makers, Pomona, CA 91768

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KALI BICHROMICUM 30C

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0310191144521	GTIN-13: 0310191144521 EAN-13: 0310191144521 GTIN-12: 310191144521 UPC-A: 310191144521 GTIN storage (14 digits): 00310191144521	92e2d518-0950-43fc-a5fc-6e03493f36ec.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10191-1445-2	2019-10-21	C162847	48780-1	956f9ecf-bcac-621f-e053-dbdaa90a74ad	KALI BICHROMICUM 30C (Potassium Dichromate)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10191-1445-2	KALI BICHROMICUM	161 in 1 VIAL, GLASS	PELLET	161		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10191-1445	KALI BICHROMICUM (POTASSIUM DICHROMATE) PELLET [REMEDY MAKERS]	1	Legacy NDC, 1 package rows	20100322_ab2e0cc5-5ac5-428a-ad76-135b853c2085.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
POTASSIUM DICHROMATE	ACTIVE INGREDIENT	T4423S18FM	1
DICHROMATE ION	ACTIVE MOIETY	9LKY4BFN2V	1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

KALI BICHROMICUM
POTASSIUM DICHROMATE
DICHROMATE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10191-1445	10191-1445-2

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
POTASSIUM DICHROMATE	T4423S18FM	ACTIB

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
3be8d685-3dba-4fd8-a68f-61fae50ef834			ab2e0cc5-5ac5-428a-ad76-135b853c2085	2010-03-22		Exact identifier spl id: 3be8d685-3dba-4fd8-a68f-61fae50ef834 spl set id: ab2e0cc5-5ac5-428a-ad76-135b853c2085

Reported adverse events (FAERS/openFDA)#

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