FDA Label for Nieapf Numbing
View Indications, Usage & Precautions
Nieapf Numbing Product Label
The following document was submitted to the FDA by the labeler of this product Jiangxi Hemei Pharmaceutical Co., Ltd. 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 4% （w/w）
Purpose
External analgesic
Use
·Temporarily relieves pain and itching due to: minor burns,sunburn, insect bites, scrapes, minor skin irritations
Warnings
For external use only.
Do Not Use
·on large areas of the body.·on broken, blistered, or abraded skin. · if allergic to local anesthetics such as lidocaine, benzocaine, or other "caine" derivatives
When Using
·avoid contact with the eyes - ·do not bandage tightly or use with heating pad -· use only as directed
Stop Use
·Condition worsens or does not improve within 7 days.·Allergic reaction occurs to ingredients in this product.·Symptom being treated does not subside or if redness,iritation
Ask Doctor
·Condition worsens or does not improve within 7 days.·Allergic reaction occurs to ingredients in this product.·Symptom being treated does not subside or if redness,iritation
Keep Oot Of Reach Of Children
lf swallowed, get medical help or contact a poison control center right away.
Directions
·Cleanse targeted skin area, pat dry. ·Apply a thin layer to the affected area, not more than 3-4 times daily.
Other Information
Store at 15-30°C(59-86°F)·Protect from excessive heat and direct sunlight-· Use only as directed
Inactive Ingredients
Water,Carbomer934, Propylene Glycol,Soybean Lecithin,.Alpha.-Tocopherol Acetate,Benzyl Alcohol.
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