Active Ingredients Purpose
Benzocaine 5.00%
Bite Relief
FDA Label NDC 64048-7336
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Product Quest Mfg. for the product Bite Relief (NDC 64048-7336). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients purpose, uses, warningfor external use only, direction, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
For temporarily relief of pain and itching associated with insect bites
Warningfor External Use Only
When using this product avoid contact with eyes and mucous membranes
Stop use and ask a doctor if condition worsens• symptoms last more than 7 days or clear up and occur again within a few days
Direction
Adults and children 2 years of age and older: • apply to the affected area nor mre than 3 to 4 times daily. Children under 2 years of age: consult a doctor
Inactive Ingredients
Acrylates/Dimethicone Copolymer
BHT
Bisabolol
C12-15 Alkyl Benzoate
Capryloyl Glycine
Caprylyl Glycol
Cedrus Atlantica Bark Extract
Cetyl Dimethicone
Chlorphenesin
Cinnamomum Zeylanicum Bark Extract
Cyclopentasiloxane
Disodium EDTA
Ethylhexyl Stearate
Ethylhexylglycerin
Glycerin
Hydrated Silica
Mannan
Neopentyl Glycol Diheptanoate
Phenoxyethanol
Polyester-7
Polyester-8
Portulaca Oleracea Extract
Propylene Glycol
Sarcosine
Sodium Polyacrylate
Steareth-100
Steareth-2
Styrene/Acrylates Copolymer
Trideceth-6
Water
Xanthan Gum
* Please review the disclaimer below.
