FDA Label for Lidocaine Hydrochloride 2%
View Indications, Usage & Precautions
Lidocaine Hydrochloride 2% Product Label
The following document was submitted to the FDA by the labeler of this product Aldermed Inc.. 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.
Active Ingredient
Lidocaine Hydrochloride 2%
Purpose
External Analgesic
Use(S)
■ For the temporary relief of pain associated with ■ Minor burns ■ Sunburn
Warnings
For External Use Only
Do Not Use
■ On wounds or damaged skin
■ In large quantities, particularly over raw surfaces or blistered areas
When Using This Product
■ Avoid contact with the eyes
■ Do not bandage tightly
Stop Use And Ask A Doctor If
■ Condition worsens
■ Symptoms persist for more than 7 days
■ Symptoms clear up and occur again within a few days
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.(1-800-222-1222)
Directions
■ 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 doctor
Other Information
• Store at room temperature
• Tamper Evident. Do not use if seal is torn, cut, or opened.
- See sachet or cartonfor lot number and expiry date
Inactive Ingredients
Acrylates/C10-30 Alkyl Acrylate Crosscopolymer, Carbomer, Glycerin, Imidurea, Methylparaben, Propylene Glycol, Propylparaben, Purified Water, Tea Tree Leaf Oil, Trolamine
Questions?
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