Kalium carbonicum 12 Special Order

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2018-04-27
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:09:26

Label at a glance#

ProductKalium carbonicum 12 Special Order

Active ingredientPOTASSIUM CARBONATE

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Kalium carbonicum 12X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Distilled water

OTC - PURPOSE SECTION

Use: Temporary relief of skin rash.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 90 DAYS OF OPENING.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KaliumCarbonicum12SOLiquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-6067-3	Kalium carbonicum 12 Special Order	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-6067	KALIUM CARBONICUM 12 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	2	Legacy NDC, 1 package rows	20180427_6014aa18-baab-4fa9-987f-4f28a545600a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
POTASSIUM CARBONATE	ACTIVE INGREDIENT	BQN1B9B9HA	1
CARBONATE ION	ACTIVE MOIETY	7UJQ5OPE7D	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Kalium carbonicum 12 Special Order
WATER
POTASSIUM CARBONATE
CARBONATE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-6067	48951-6067-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
POTASSIUM CARBONATE	BQN1B9B9HA	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
6ad48609-b121-ecf3-e053-2991aa0ad704			6014aa18-baab-4fa9-987f-4f28a545600a	2018-04-27	Warnings	Exact identifier spl id: 6ad48609-b121-ecf3-e053-2991aa0ad704 spl set id: 6014aa18-baab-4fa9-987f-4f28a545600a

Reported adverse events (FAERS/openFDA)#

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