Indications & Usage
Directions: FOR TOPICAL USE ONLY.
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Arnica Nettle (NDC 48951-1401). 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.
Directions: FOR TOPICAL USE ONLY.
Apply gel to skin as soon as possible. Reapply several times daily. Under age 2: Consult a doctor
Active Ingredients: 100 gm contains: 9 gm Urtica urens (Small nettle) 1X, 3 gm Arnica 1X, 2gm Calendula 1X, 2 gm Thuja e summ. (American arborvitae) 1X, 2 gm Symphytum (Comfrey) 1X, 1 gm Cantharis (Spanish fly) 3X
Inactive Ingredients: Distilled water, Glycerin, Organic cane alcohol, Boric acid, Sodium alginate, Sodium hydroxide, Aloe vera, Cajeput oil, Larch resin, Rosemary oil, Sorbic acid, Tea tree oil, Thyme oil, Grapefruit seed extract, Colloidal silver
Uses: Temporary relief of burns, sunburn, insect bites, bee stings and rashes.
KEEP OUT OF REACH OF CHILDREN.
Warnings: FOR EXTERNAL USE ONLY.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.
FOR BURNS, SEEK MEDICAL ATTENTION IF NEEDED.
Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
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