Exsel Aloe
FDA Label NDC 55301-016

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 Exsel Aloe (NDC 55301-016). 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, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Lidocaine HCl   0.5%


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

  • condition worsens or if symptoms persist 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 areas 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. (226 g)


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