FDA Label for 999 Itch Relief
View Indications, Usage & Precautions
999 Itch Relief Product Label
The following document was submitted to the FDA by the labeler of this product China Resources Sanjiu Medical & 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 Ingredients
Menthol 1%
Camphor (synthetic) 1%
Dexamethasone Acetate 0.075%
Purpose
External Analgesic
External Analgesic
Anti-allergic
Warnings
For external use only. Avoid contact with the eyes. If swallowed, get medical help or contact a Poison Control Center right away.
Keep out of reach of children.
Stop Use And Seek Medical Advice If
Condition worses. Symptoms persisit for more than 7 days. Symptoms clear up and occur again within a few days. Excessive irritation of the skin develops.
Directions
Pregnant and children under 2 years of age. Do not use, consult a doctor.
Adult and children 2 years of age and older. Apply liberally to affected area not more than 5 times daily and 5-8 times per day for some severe cases or follow doctor's instruction.
Other Information
Keep in a lightly closed container. Store at 8 to 30 degree centigrade (46-86 Fahrenheit) in a dry plac away from sunlight.
Inactive Ingredients
Hexadecanolactone
Ethylparaben
Glycerin
Glycertyl Monostearate
Drug Facts
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