FDA Label for Dch Pain Relief
View Indications, Usage & Precautions
Dch Pain Relief Product Label
The following document was submitted to the FDA by the labeler of this product Derma Care Research Labs, 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
Lidocaine 4%
Otc - Purpose
External Analgesic.
Dosage & Administration
For the temporary relief of pain and itching due to sunburn, minor burns, insect bites, minor cuts, scrapes, and minor skin irritations.
Warnings
For external use only.
Flammable--Do not use while smoking or near heat or flame.
Do not use in large quantities, particularly over raw surfaces or blistered areas.
When using this product avoid contact with eyes. Rinse eyes with water to remove. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120F.
Stop use and ask a doctor if the condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days, irritation develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If the product is swallowed, get medical help or contact a Poison Control Center right away.
Indications & Usage
Adults and children 2 years and older: apply to the affected area, not more than 3 to 4 times a day. Children under 2 years of age: consult a physician. To apply to face, squeeze into palm of hand and gently apply.
Inactive Ingredient
Water, Glycerin, Alcohol Denat., Propylene Glycol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Chamomilla Recutita (Matricaria) Flower Extract, Cucumis Sativus (Cucumber) Fruit Extract, Disodium EDTA, Triethanolamine, Diazolidinyl Urea, Simethicone.
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