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Sunburn relief gel - Medication Information

Product NDC Code 72288-005
Drug Name

Sunburn relief gel

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine hydrochloride 5 mg/g
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 1011849
Application Number M017
Labeler Name Amazon.com Services LLC
Packages
Package NDC Code Description
72288-005-34 226 g in 1 bottle, pump (72288-005-34)
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Adverse reactions

Information about undesirable effects, reasonably associated with use of the drug, that may occur as part of the pharmacological action of the drug or may be unpredictable in its occurrence. Adverse reactions include those that occur with the drug, and if applicable, with drugs in the same pharmacologically active and chemically related class. There is considerable variation in the listing of adverse reactions. They may be categorized by organ system, by severity of reaction, by frequency, by toxicological mechanism, or by a combination of these.
Adverse reaction "Alexa, reorder Amazon Basics Sunburn Relief Gel." alexa Distributed by: Amazon.com Services LLC Seattle, WA 98109 1-877-485-0385 ©2024 Amazon.com Services, LLC. or its affiliates www.amazon.com/amazonbasics

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Lidocaine HCl 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 not 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 water, propylene glycol, glycerin, Aloe Barbadensis Leaf Juice, sodium hydroxide, isopropyl alcohol, polysorbate 80, carbomer, phenoxyethanol, benzyl alcohol, menthol, disodium EDTA, blue 1, 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.
Sunburn Relief Gel Lidocaine HCl WATER PROPYLENE GLYCOL GLYCERIN ALOE VERA LEAF SODIUM HYDROXIDE ISOPROPYL ALCOHOL POLYSORBATE 80 CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE PHENOXYETHANOL BENZYL ALCOHOL MENTHOL EDETATE DISODIUM FD&C BLUE NO. 1 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.
Principl display panel amazon basics sunburn relief gel Pain Relieving Gel with Aloe Vera and Lidocaine HCl NET WT 8 OZ (226 g) image description

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use in large quantities, particularly over raw surfaces or blistered areas

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.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clean up and occur again within a few days

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product avoid contact with the eyes

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

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