Description
Water-based suspension, dietary supplement Oral Spray
Artemic Rescue
FDA Label NDC 83278-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Amc Pharma Llc for the product Artemic Rescue (NDC 83278-001). 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 description, otc - active ingredient, inactive ingredient, dosage & administration, instructions for use, warnings, otc - keep out of reach of children, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Curcuma Longa Extract, Boswellia SerrataExtract, Antioxidant Artemisinin,Vitamin C (L-Ascorbic Acid)
Inactive Ingredient
Water, Vegetable Castor Oil, Natural Propanediol, DL-Alpha-Tocopherol
Dosage & Administration
5 sprays provides 1 ml of ArtemiC. Servings per container: 4
Instructions For Use
Shake well before using. Adults apply 5 sprays, twice daily in the mouth, morning and evening for 2 consecutive days.preferably at least half hour before eating.
Warnings
Keep out of reach of children. Not intended for pregnant or nursing woman. Discontinue use or consult your doctor if any adverse reactions occur. Do not use if inner bottle or spray cap is broken, or shows sign of tampering.
Otc - Keep Out Of Reach Of Children
Keep Out of Reach of Children.
Storage And Handling
Store in a dry, cool place and avoid heat and direct sunlight. Do not exceed temperatures above 77 deg F. Usable until expiration date. Once opened, use witjin 1 month. Do not freeze.
Indications & Usage
Adults apply 5 sprays, twice daily, into mouth.
Otc - Purpose
Dietary supplement to support the immune system.
Package Label.Principal Display Panel
NDC 83278-001-05
Bottle label NDC 83278-001-05
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