Indications & Usage
Directions: FOR TOPICAL USE ONLY.
Archangelica Eucalyptus
FDA Label NDC 48951-1072
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 Archangelica Eucalyptus (NDC 48951-1072). 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.
Otc - Active Ingredient
Active Ingredient: 100 gm contains: 10 gm Archangelica (Longwort) 1X, 30 gm Oleum Eucalypti (Eucalyptus oil) 1X
Inactive Ingredient
Inactive Ingredients: Organic olive oil, Distilled water, Lanolin, Beeswax, Glyceryl monostearate, Stearyl alcohol, Potassium sorbate, Polyoxyl 40 stearate, Grapefruit seed extract
Otc - Purpose
Use: Temporary relief of cough
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: FOR EXTERNAL USE ONLY.
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.
Otc - Questions
Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com
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