Exchange Select Burn Relief
FDA Label NDC 55301-044

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Army And Air Force Exchange Service for the product Exchange Select Burn Relief (NDC 55301-044). 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 ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Lidocaine HCl 0.50%

Purpose

Topical Analgesic

Uses

  • temporary relief of pain and itching
  • helps relieve and soothes pain from sunburn, minor burns, cuts, scrapes, skin irritations and insect bites

Warnings

For external use only

Do not use in large quantities, particularly over raw surfaces or blistered areas.

When Using This Product

  • avoid contact with eyes.

Stop Use And Ask A Doctor If

  • conditions worsens or symptoms persists for more than 7 days.
  • symptoms 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 2 years of age and older.apply to affected area not more than 3 to 4 times daily
  • children under 2 years of age: do not use, ask a doctor.

Inactive Ingredients

Water, Propylene Glycol, Glycerin, Isopropyl Alcohol, Triethanolamine, Polysorbate 80, Carbomer, Aloe Barbadensis Leaf Juice Powder, Menthol, Disodium EDTA, Diazolidinyl Urea, Yellow 5, Blue 1.

Principal Display Panel

exchange

select

X

BURN RELIEF

Pain Relieving Gel

with
Lidocaine
Cools, Soothes and
Relieves Sunburned Skin

NET WT 8 OZ (227 g)
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