Label at a glance#

ProductKali carbonicum

Active ingredientPOTASSIUM CARBONATE

Label structure9 sections

Indications and uses

To relieve the symptoms of sour belching.

Dosage and administration

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

KALI CARB

USES

OTC - PURPOSE SECTION

To relieve the symptoms of sour belching.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

Indications:

KALI CARB Sour Belching

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

RECENT MAJOR CHANGES SECTION

Indication: Sour Belching

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The OTC potency range of KALI CARB is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

Kalicar2023

All WHP single remedies are made to order; thus, the labels are printed on the same label stock as the orders are filled.

‘Bottle Size’ and ‘Potency’ vary on the label depending on customer choice.

Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68428-451-03	2025-01-30	C162847	48780-1	2cef2736-9ffe-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-451-05	2025-01-30	C162847	48780-1	2cef2736-9ffe-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-451-06	2025-01-30	C162847	48780-1	2cef2736-9ffe-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-451-11	2025-01-30	C162847	48780-1	2cef2736-9ffe-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-451-12	2025-01-30	C162847	48780-1	2cef2736-9ffe-d83d-e063-dadaa90ab31f	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68428-451-03	Kali carbonicum	75 in 1 VIAL, GLASS	PELLET	75	5
68428-451-05	Kali carbonicum	150 in 1 VIAL, GLASS	PELLET	150	5
68428-451-06	Kali carbonicum	1200 in 1 BOTTLE, GLASS	PELLET	1200	5
68428-451-11	Kali carbonicum	300 in 1 BOTTLE, GLASS	PELLET	300	5
68428-451-12	Kali carbonicum	600 in 1 BOTTLE, GLASS	PELLET	600	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68428-451	KALI CARBONICUM (POTASSIUM CARBONATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	5	Legacy NDC, 5 package rows	20231020_56ba7f2a-8778-4c9f-8e87-386f597017bb.zip

Products#

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

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

Kali carbonicum
POTASSIUM CARBONATE
LACTOSE
CARBONATE ION
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68428-451	68428-451-03, 68428-451-05, 68428-451-11, 68428-451-12, 68428-451-06

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
Name	UNII	Kind
LACTOSE	J2B2A4N98G	IACT
POTASSIUM CARBONATE	BQN1B9B9HA	ACTIB
SUCROSE	C151H8M554	IACT

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
0812f0c1-ccc2-6586-e063-6394a90a4999			56ba7f2a-8778-4c9f-8e87-386f597017bb	2023-10-19	Warnings	Exact identifier spl id: 0812f0c1-ccc2-6586-e063-6394a90a4999 spl set id: 56ba7f2a-8778-4c9f-8e87-386f597017bb

Reported adverse events (FAERS/openFDA)#

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