FDA Label for Myderm Bite Relief
View Indications, Usage & Precautions
Myderm Bite Relief Product Label
The following document was submitted to the FDA by the labeler of this product Inspec Solutions Llc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredient:
Benzocaine - 5.0%
Otc - Purpose
Benzocaine - 10.0% ............Pain Relief
Indications & Usage
Temporary relief of pain and itching associated with insect bites
Warnings
For external use only
When using this product • avoid contact with the eye
Otc - Stop Use
Stop use and ask a doctor if • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Direction Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
Children under 2 years of age: consult a physician
Inactive Ingredient
Aloe Barbadensis Leaf Extract
Camphor
Chamomilla Recutita (Matricaria) Flower Extract
Diazolidinyl Urea
Disodium EDTA
Eugenia Caryophyllus (Clove) Flower Oil
Hydrocortisone
Inactive Ingredients:
Mentha Piperita (Peppermint) Oil
Menthol
Methylparaben
Olea Europaea (Olive) Fruit Oil
Papain
PEG-2 Stearate
PEG-2 Stearate SE
Polyethylene
Propylene Glycol
Propylparaben
SD Alcohol 40
Water
Package Label.Principal Display Panel
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