ANTIMONIUM TARTARICUM

Manufacturer: Remedy Makers
Effective date: 2010-01-28
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:02:10

Label at a glance#

ProductANTIMONIUM TARTARICUM

Active ingredientANTIMONY POTASSIUM TARTRATE

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

ANTIMONIUMTARTARICUM30C

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0310191184527	GTIN-13: 0310191184527 EAN-13: 0310191184527 GTIN-12: 310191184527 UPC-A: 310191184527 GTIN storage (14 digits): 00310191184527	53d5e3da-bb1a-422d-a1bb-dc8662f6b204.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10191-1845-2	2019-10-21	C162847	48780-1	956f9ecf-d2ae-621f-e053-dbdaa90a74ad	ANTIMONIUM TARTARICUM 30C (Antimony Potassium Tartrate)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10191-1845-2	ANTIMONIUM TARTARICUM	167 in 1 VIAL, GLASS	PELLET	167		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10191-1845	ANTIMONIUM TARTARICUM (ANTIMONY POTASSIUM TARTRATE) PELLET [REMEDY MAKERS]	1	Legacy NDC, 1 package rows	20100128_c3ea165d-6ca5-429e-99a7-59bf449538cc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
ANTIMONY POTASSIUM TARTRATE	ACTIVE INGREDIENT	DL6OZ476V3	1
ANTIMONY CATION (3+)	ACTIVE MOIETY	069647RPT5	1

Products#

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

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

ANTIMONIUM TARTARICUM
ANTIMONY POTASSIUM TARTRATE
ANTIMONY CATION (3+)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10191-1845	10191-1845-2

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
ANTIMONY POTASSIUM TARTRATE	DL6OZ476V3	ACTIB

Source Document#

Source XML · Source PDF

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
dd13a759-7821-43e7-b8a5-81ddb86ed320			c3ea165d-6ca5-429e-99a7-59bf449538cc	2010-01-28		Exact identifier spl id: dd13a759-7821-43e7-b8a5-81ddb86ed320 spl set id: c3ea165d-6ca5-429e-99a7-59bf449538cc

Reported adverse events (FAERS/openFDA)#

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