Burn Relief

Manufacturer: Product Quest Mfg
Effective date: 2018-07-23
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:56:23

Label at a glance#

ProductBurn Relief

Active ingredientLidocaine

Label structure7 sections

Indications and uses

Temporarily relieves pain and itching due to • sunburn • minor burns • minor cuts • scrapes • insect bites • minor skin irritation

Dosage and administration

• shake well • 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 • to apply to face, spray into palm of hand and gently apply

Contacts and useful links#

PhoneLabel contact1-866-483-2846

Label contents#

Full prescribing information#

Active ingredient Purpose

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 0.5% External analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves pain and itching due to

• sunburn • minor burns • minor cuts • scrapes

• insect bites • minor skin irritation

Warnings

WARNINGS SECTION

For external use only

Flammable: Do not spray while smoking or near heat or flame

SPL UNCLASSIFIED SECTION

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

OTC - DO NOT USE SECTION

When using this product

OTC - WHEN USING SECTION

keep out of your eyes
use only as directed
do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120F.

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition gets worse
symptoms last more than 7 days
symptoms clear up and occur again within a few days

Keep out of reach of the children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

• shake well
• 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

• to apply to face, spray into palm of hand and gently apply

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Carbomer, Diazolidinyl Urea, Disodium Cocoamphodipropionate, Disodium EDTA, Glycerin, Methylparaben, Propylene Glycol, Propylparaben, SD Alcohol 40, Simethicone, Tocopheryl Acetate, Triethanolamine

Questions and comments?

OTC - QUESTIONS SECTION

1-866-483-2846

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1442274	lidocaine 0.5 % Topical Spray	PSN	1
1442274	lidocaine 5 MG/ML Topical Spray	SCD	1
1442274	lidocaine 0.5 % Topical Spray	SY	1

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
LIDOCAINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64048-5115-4	2020-01-31	C162847	48780-1	9d75b9d0-e707-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64048-5115-4	Burn Relief	127 g in 1 CAN	spray	127		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64048-5115	BURN RELIEF (LIDOCAINE 0.5%) SPRAY [PRODUCT QUEST MFG]	1	Legacy NDC, 1 package rows	20180723_ca7ed548-9d8a-4138-a49c-1b6b2e008cef.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Burn Relief
Lidocaine 0.5%
Lidocaine
ALOE VERA LEAF
Diazolidinyl Urea
Disodium Cocoamphodipropionate
EDETATE DISODIUM
Glycerin
Methylparaben
Propylene Glycol
Propylparaben
ALCOHOL
.ALPHA.-TOCOPHEROL ACETATE
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64048-5115	64048-5115-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Lidocaine	98PI200987	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	IACT
Diazolidinyl Urea	H5RIZ3MPW4	IACT
Disodium Cocoamphodipropionate	6K8PRP397M	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
Glycerin	PDC6A3C0OX	IACT
Methylparaben	A2I8C7HI9T	IACT
Propylene Glycol	6DC9Q167V3	IACT
Propylparaben	Z8IX2SC1OH	IACT
ALCOHOL	3K9958V90M	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
TROLAMINE	9O3K93S3TK	IACT

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0cbb13d2-b85f-41b4-adcf-d552ea809f90			ca7ed548-9d8a-4138-a49c-1b6b2e008cef	2018-07-23	Warnings	Exact identifier spl id: 0cbb13d2-b85f-41b4-adcf-d552ea809f90 spl set id: ca7ed548-9d8a-4138-a49c-1b6b2e008cef

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.