Active Ingredient
ANTIMONIUM TART
Antimonium Tartaricum Pellet
FDA Label NDC 71919-829
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Washington Homeopathic Products for the product Antimonium Tartaricum (NDC 71919-829). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, uses, keep out of reach of children, indications, stop use and ask doctor, directions, inactive ingredient section, package label display, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Indicated for loose cough
Keep Out Of Reach Of Children
As with all medicines, keep out of reach of children.
Indications
ANTOMONIUM TART Loose cough
Stop Use And Ask Doctor
If symptoms worsen or persist for more than 7 days, or if pregnant or nursing, consult a licensed practitioner.
Directions
Directions: Adults & children: Dissolve 4 pellets under the tongue 3 times a day or as directed by a licensed practitioner. Other information: Do not use if seal is broken.
Inactive Ingredient Section
SUCROSE/LACTOSE
Package Label Display
The OTC potency range of ANTIMONIUM TART is 30C – 200C.
Availability is subject to change.
Antimoniumtart (Antimon Tart)
* Please review the disclaimer below.
