Bed Bug Instant Bite Relief Gel
FDA Label NDC 70466-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by P.f. Harris Mfg. Co. Llc for the product Bed Bug Instant Bite Relief (NDC 70466-001). 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 drug facts, active ingredients, purpose, uses:, directions:, warnings:, do not use, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Lidocaine 4%
Purpose
Topical Anesthetic
Uses:
For the temporary relief of discomfort and pain associated with • minor burns and skin irritations • minor cuts and scrapes • itching.
Directions:
Adults and children 12 years of age and older: Apply to affected area not more than 3-4 times daily.
Warnings:
For external use only. Avoid contact with the eyes.
Do Not Use
in large quantities, particularly over raw or blistered areas.
Stop Use And Ask A Doctor If
•skin becomes irritated • condition worsens or sysmptoms last than 7 days • symptoms clear up and recur within a few days.
Inactive Ingredients:
Aloe Barbadensis Leaf Juice, Calendula Officinalis Flower Extract, Camellia Sinensis (Green Tea) Leaf Extract, Carbomer, Chamomilla Recutita (Matricaria) Flower Extract, Diazolidinyl Urea, Disodium EDTA, Glycerin, Menthol, Methylparaben, Propylene Glycol, Propylparaben, Purified Water, SD Alcohol 40-2, Symphytum Officinale (Comfrey) Leaf Extract, Triethanolamine
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