Indications & Usage
Directions: FOR TOPICAL USE ONLY
Arnica Calendula Wound Powder
FDA Label NDC 48951-1402
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy, Inc for the product Arnica Calendula Wound (NDC 48951-1402). 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 indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Apply to skin as needed. Under age 2: Consult a doctor.
Otc - Active Ingredient
Active Ingredients: 100gm contains: 25gm Arnica montana MT, 16.5gm Calendula ex herba MT, 16.6gm Echinacea angustifolia MT (Purple coneflower), 1gm Silicea (Quartz), 1gm Stibium metallicum (Antimony)
Inactive Ingredient
Inactive Ingredient: Diatomaceous Earth
Prepared using rhythmical processes.
Otc - Purpose
Use: Temporary relief of superficial wounds and eczema.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains lactose. 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.
Otc - Questions
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:
* Please review the disclaimer below.
