Active Ingredient
ANTIMONIUM CRUDUM HPUS 3X and Higher
Antimonium Crudum
FDA Label NDC 15631-0513
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc for the product Antimonium Crudum (NDC 15631-0513). 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, indications, dosage, warnings, otc - stop use, otc - pregnancy or breast feeding, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Irritability, Eczema, Warts
Indications
Condition listed above or as directed by the physician.
Dosage
Adults- Take 4 or 6 Tablets by mouth, three times daily or as suggested by physician. Children 2 years and older- take 1/2 the adult dose.
Warnings
This product is to be used for self-limiting conditions
Otc - Stop Use
If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional
Otc - Pregnancy Or Breast Feeding
As with any drug, if you are pregnant, or nursing a baby, seek professional advice before taking this product
Otc - Keep Out Of Reach Of Children
Keep this and all medication out of reach of children
Otc - Do Not Use
Do not use if capseal is broken or missing.
Close the cap tightly after use.
Inactive Ingredients
Lactose
Storage
Store in a cool dark place
Questions Or Comments
www.Rxhomeo.com | 1.888.2796642 | [email protected]
Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758
Package Label.Principal Display Panel
Image Description (15631 0513)
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