Purpose
Uses: Temporarily relieves symptoms of burns, sunburn, insect bites, bee stings, poison oak or poison ivy rashes, chicken pox and hives.
Arnica Nettle Burn And Bite
FDA Label NDC 48951-1149
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 Nettle Burn And Bite (NDC 48951-1149). 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 purpose, dosage & administration, otc-active ingredient, inactive ingredient, keep out of reach of children, do not use section, ask doctor section, pregnancy or breast feeding section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Directions: Take 1-2 sprays up to every hour. Under age 2: Ask a doctor.
Otc-Active Ingredient
Active Ingredients: Urtica urens 1X HPUS, Arnica e flor. 2X HPUS, Calendula 2X HPUS, Thuja e summ. 2X HPUS, Symphytum 2X HPUS, Cantharis ex animale 7X HPUS, Colloidal silver 7X HPUS.
Inactive Ingredient
Inactive Ingredients: Water, Organic grain alcohol.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Do Not Use Section
Warnings: Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.
Ask Doctor Section
Consult a doctor for burns or if symptoms worsen or persist.
Pregnancy Or Breast Feeding Section
If you are pregnant or nursing, consult a doctor before use.
Questions Section
Questions? Uriel Pharmacy
866 642-2858 East Troy, WI 53120
www.urielpharmacy.com
Principal Display Panel
Arnica Nettle
Burn and Bite Spray
Homeopathic
net vol. 30 ml (1 fl. oz.)
Arnica Nettle Spray Bottle Label (Arnnets01)
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