FDA Label for Dermfree Anti-itch
View Indications, Usage & Precautions
Dermfree Anti-itch 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
Hydrocortisone acetate 1%
Purpose
Anti-itch
Use
temporarily relieves pain and itching associated with:
▇insect bites▇ minor burns ▇sunburn▇ minor skin irritations▇ minor cuts ▇scrapes▇ rashes due to poison ivy, poison oak, and poison sumac ▇dries the oozing and weeping of poison ivy, poison oak ，and poison sumac
Warnings
For external use only.
Do Not Use
▇on large areas of the body
▇with any other product containing diphenhydramine, even one taken bymouth
Stop Use
▇condition worsens or does not improve within 15 days
▇symptoms persist for more than 15 days or clear up and occur again withina few days
Ask Doctor
▇on chicken pox
▇ on measles
Keep Oot Of Reach Of Children
lf swallowed, get medical help or contact aPoison control center right away.
Directions
▇do not use more than directed
▇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: ask a doctor
Other Information
▇protect from excessive heat (40°C/104°F)
Inactive Ingredients
Purified water、Ethanol 95%、Ethyl paraben、C18-16 Alcohol、 Mono- and di-glycerol fatty acid esters、 Fatty alcohol polyoxyethylene ether、Liquid paraffin
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