FDA Label for Anti-itch

View Indications, Usage & Precautions

Anti-itch Product Label

The following document was submitted to the FDA by the labeler of this product Navarro Discount Pharmacies,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.

Active Ingredients (In Each Gram)



Diphenhydramine HCl 2%


Purposes



Topical analgesic

Skin protectant


Uses



  • temporarily relieves itching and pain associated with insect bites, minor skin irritations and rashes due to poison ivy, poison oak or poison sumac
  • dries the oozing and weeping of poison ivy, poison oak, and poison sumac

Warnings



For external use only


Do Not Use



  • on chicken pox or measles
  • with any other product containing diphenhydramine, even one taken by mouth
  • on large areas of the body, including large areas of poison ivy, sunburn, or broken, blistered or oozing skin

Stop Use And Ask A Doctor If



  • condition worsens or does not improve within 7 days
  • symptoms persist for more than 7 days or 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


Directions



  • adults and children 12 years of age and over:  apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age:  ask a doctor
  • do not use more often than directed

Other Information



  • store at 15°-25°C (59°-77°F)

Inactive Ingredients



camphor, citric acid, ethanol, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate


Package Label



Anti-Itch Gel


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