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Rite Aid Burn Relief

Medically reviewed on December 4, 2017

Dosage form: gel
Ingredients: LIDOCAINE HYDROCHLORIDE 0.5g in 100g
Labeler: RITE AID CORPORATION
NDC Code: 11822-9009

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active IngredientLidocaine HCl 0.50%

Purpose

Topical Anesthetic

Uses
  • temporary pain 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 if 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

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

Principal Display Panel

RITE AID
BURN RELIEF
ALOE VERA GEL
Cools and Relieves Sunburn Pain
with LIDOCAINE
NET WT 8 OZ (227 g)


RITE AID BURN RELIEF 
lidocaine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-9009
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER 
TROLAMINE 
ISOPROPYL ALCOHOL 
EDETATE DISODIUM 
ALOE VERA LEAF 
PROPYLENE GLYCOL 
GLYCERIN 
POLYSORBATE 80 
DIAZOLIDINYL UREA 
MENTHOL 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:11822-9009-6226 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/03/2012
Labeler - RITE AID CORPORATION (014578892)

 
RITE AID CORPORATION

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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