FDA.reportPublic FDA data

Burn Relief - CVS Pharmacy, Inc.

Manufacturer
CVS Pharmacy, Inc.
Effective date
2026-04-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:52:44

Label at a glance#

ProductBurn Relief
Active ingredientLIDOCAINE
Label structure9 sections

Indications and uses

for the temporary relief of pain and itching associated with: minor burns minor cuts insect bites sunburn scrapes minor skin irritations

Dosage and administration

adults and children 2 years of age andolder: spray to affected area not more than 3 to 4 times daily children under 2 years of age: do not use, consult a doctor.

Label contents#

Full prescribing information#

​Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of pain and itching associated with:

  • minor burns
  • minor cuts
  • insect bites
  • sunburn
  • scrapes
  • minor skin irritations

Warnings

WARNINGS SECTION

For external use only.

Extremely Flammable:

SAFE HANDLING WARNING SECTION

Keep away from fire, sparks, and heated surfaces. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F.

Do not use

OTC - DO NOT USE SECTION

in large quantities, particularly over raw surfaces or blistered areas.

When using this product

OTC - WHEN USING SECTION

  • avoid spraying in eyes
  • use only as directed
  • intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal
  • do not bandage or apply local heat (such as heating pads) or a medicated patch to area of use

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • ask a health professional before use

Keep out of reach of 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

  • adults and children 2 years of age andolder: spray to affected area not more than 3 to 4 times daily
  • children under 2 years of age: do not use, consult a doctor.

Other information

OTHER SAFETY INFORMATION

store at 20° to 25°C (68° to 77°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Isobutane, SD Alcohol 40-B, Propylene Glycol, Caprylic/Capric Triglyceride, Calendula Officinalis Flower Extract, Arnica Montana Flower Extract,Anthemis Nobilis Flower Oil, Water,Glycerin.

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS

Fast-Acting

BURN RELIEF
SPRAY

Lidocaine 4%
External Analgesic

Compare to Solarcaine® Burn Pain
Relief Spray active ingredientt

Long-Lasting Numbing Relief
Cools, Moisturizes & Soothes
Sunburned Skin

Maximum Strength
Burn & Pain Relief+

Chamomile
Flower Scent

NET WT 4 OZ (113 g)

*Maximum % lidocaine allowed
per the external analgesic monograph.

cartoncarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1869797lidocaine 4 % Topical SprayPSN2
1869797lidocaine 40 MG/ML Topical SpraySCD2
1869797lidocaine 4 % Topical SpraySY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51316-501-04Burn Relief113 g in 1 CANAEROSOL, SPRAY1132

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51316-50151316-501-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANTHEMIS NOBILIS FLOWER OILUB27587839IACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
ARNICA MONTANA FLOWER WATERU7L2JP51PRIACT
GLYCERINPDC6A3C0OXIACT
LIDOCAINE98PI200987ACTIB
ISOBUTANEBXR49TP611IACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Burn ReliefLIDOCAINECVS Pharmacy, Inc.42b3c341-f422-b2b4-e063-6294a90a47b22026-04-06WarningsExact identifier
ndc (package): 51316-501-04
ndc (product): 51316-501
ndc11 (package): 51316050104
spl id: 4ddebe1a-2d43-a482-e063-6394a90ab66d
spl set id: 42b3c341-f422-b2b4-e063-6294a90a47b2

Reported adverse events (FAERS/openFDA)#

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