EmuAid
EmuAid is an FDA drug label for the active ingredient SILVER manufactured by Speer Laboratories, LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20210114.
Generic: SILVER
Manufacturer: Speer Laboratories, LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 55926-0024
Application:
Effective: 20210114
Active Ingredients: Active Ingredient Argentum Metallicum 10x, 20x, 30 HPUS* * HPUS indicates that this ingredient is officially a part of the Homeopathic Pharmacopia of the United States
Indications & Usage
Indications for Use For the relief of these symptoms due to minor wounds and burns, bruises, ulcerations, sunburn, razor burn, scrapes, rashes, blisters, bug bites, and skin eruptions from acne, eczema, or minor infection: • burning • stinging • itching • redness • stiffness • minor pain • minor inflammation
Dosage & Administration
Directions Apply a thin layer of Emuaid over affected area, and repeat 3-4 times daily or as needed to relieve symptoms.
Contraindications
Not available.
Warnings
Warnings For external use only. If skin condition persists after 7 days, or returns, consult a physician immediately.
Adverse Reactions
Not available.
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Speer Laboratories, LLC