FDA.reportPublic FDA data

WAG Aftrsn Burn Relief Spray 8oz

Manufacturer
Walgreen Company
Effective date
2017-10-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:53:09

Label at a glance#

ProductWALG AFTRSN BURN RELIEF
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

Temporary relief of pain and itching Helps to relieve and soothe pain from sunburn, minor burns, skin irritations, scrapes, insect bites.

Dosage and administration

Adults and children 2 years or older: apply to affected area not more than 3-4 times daily. Children under 2 years of age: do not use; ask a doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Product

WALGREENS AFTERSUN BURN RELIEF SPRAY

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine Hydrochloride 0.5%

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Uses:

INDICATIONS & USAGE SECTION

  • Temporary relief of pain and itching
  • Helps to relieve and soothe pain from sunburn, minor burns, skin irritations, scrapes, insect bites.

Warnings:

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

in large quantities, particularly over raw surfaces or areas with blisters.

When using this product:

OTC - WHEN USING SECTION

  • Avoid contact with eyes.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

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 or older: apply to affected area not more than 3-4 times daily.
  • Children under 2 years of age: do not use; ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Glycerin, Propanediol, Aloe Barbadensis Leaf Juice, Carbomer, Tocopherol Acetate, PEG-40 Hydrogenated Castor Oil, Sodium Lauroyl Sarcosinate, Disodium EDTA, Phenoxyethanol, Sodium Hydroxide

Questions or comments?

OTC - QUESTIONS SECTION

www.walgreens.com or call toll free 1-800-XXX-XXXX

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens
Sunburn Relief
CONTINUOUS SPRAY
LIDOCAINE 0.5% /
EXTERNAL ANALGESIC
PAIN RELIEF
LIDOCAINE
8 OZ (227 g)

Walgreens Sunburn Relief CONTINUOUS SPRAY LIDOCAINE 0.5% / EXTERNAL ANALGESIC PAIN RELIEF LIDOCAINE 8 OZ (227 g)Walgreens Sunburn Relief CONTINUOUS SPRAY LIDOCAINE 0.5% / EXTERNAL ANALGESIC PAIN RELIEF LIDOCAINE 8 OZ (227 g)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1010931lidocaine HCl 0.5 % Topical SprayPSN2
1010931lidocaine hydrochloride 5 MG/ML Topical SpraySCD2
1010931lidocaine hydrochloride 0.5 % 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
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-9919-362020-09-27C16284748780-1ab0e2407-29c7-f274-e053-dbdaa90a6471WAG Aftrsn Burn Relief Spray 8oz
0363-9919-362020-09-25C16284748780-1ab0e2407-29c7-f274-e053-dbdaa90a6471WAG Aftrsn Burn Relief Spray 8oz
0363-9919-362020-07-22C16284748780-1ab0e2407-29c7-f274-e053-dbdaa90a6471WAG Aftrsn Burn Relief Spray 8oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-9919-36WALG AFTRSN BURN RELIEF237 mg in 1 BOTTLESPRAY2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-9919WALG AFTRSN BURN RELIEF (LIDOCAINE HYDROCHLORIDE) SPRAY [WALGREEN COMPANY]2Legacy NDC, 1 package rows20171130_de3e40b5-0c2d-45d6-a8fb-17e9a1041c0e.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-99190363-9919-36

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
SODIUM LAUROYL SARCOSINATE632GS99618IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM HYDROXIDE55X04QC32IIACT

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
e8dd78fa-e537-4523-833d-21d554912d4ade3e40b5-0c2d-45d6-a8fb-17e9a1041c0e2017-10-05WarningsExact identifier
spl id: e8dd78fa-e537-4523-833d-21d554912d4a
spl set id: de3e40b5-0c2d-45d6-a8fb-17e9a1041c0e

Reported adverse events (FAERS/openFDA)#

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