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Equate burn relief - Medication Information

Product NDC Code 79903-237
Drug Name

Equate burn relief

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine hydrochloride .5 g/100g
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 1011849
Application Number M017
Labeler Name Walmart Inc
Packages
Package NDC Code Description
79903-237-08 226 g in 1 bottle (79903-237-08)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Lidocaine HCI 0.5%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions adults and children 2 years of age and older: apply to affected area no more than 3 to 4 times daily children under 2 years of age: ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Aloe Barbadensis Leaf Juice, Blue 1, Carbomer, Disodium EDTA, Ethylhexylglycerin, Glycerin, Maltodextrin, Menthol, Phenoxyethanol, Polysorbate 20, Propanediol, SD Alcohol, Sodium Hydroxide, Water, Yellow 5

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses for the temporary relief of pain and itching associated with minor burns sunburn minor cuts scrapes insect bites minor skin irritations

Purpose

Information about the drug product’s indications for use.
Purpose External analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
equate Burn Relief LIDOCAINE HYDROCHLORIDE WATER ALOE FD&C BLUE NO. 1 CARBOMER 934 DISODIUM HEDTA ETHYLHEXYLGLYCERIN MENTHOL MALTODEXTRIN PHENOXYETHANOL POLYSORBATE 20 PROPANEDIOL ALCOHOL SODIUM HYDROXIDE FD&C YELLOW NO. 5 LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE HYDROCHLORIDE ANHYDROUS

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
image description image description

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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 or clearup and occur again within a few days

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API