Active Ingredients
antimonium tartaricum 12x,30x,200c,1m
Total Antimony
FDA Label NDC 61657-0966
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by White Manufacturing Inc. Dba Micro -west for the product Total Antimony (NDC 61657-0966). 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 ingredients, uses, keep out of reach of children, indications, ask doctor, directions, inactive ingredient, other, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Metallic taste, gout-like symptoms, angina, anorexia, fatigue, myopathy, hypotension,
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Indications
INDICATIONS: Metallic taste, gout-like symptoms, angina, anorexia, fatigue, myopathy, hypotension, "antimony spots" if exposed to vapor
Ask Doctor
If pregnant or nursing, please consult physician before using this product
Directions
Directions: Orally 6 drops, 4 times a day
Inactive Ingredient
Not more than 20% Alcohol
Other
Manufactured for Micro West
Douglas, WY 82633
1-307-358-5066
* Please review the disclaimer below.
