Antiseptic Pain Relieving

Manufacturer
Walgreens | Product Quest Mfg
Effective date
2018-04-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:17

Label at a glance#

ProductAntiseptic Pain Relieving
Active ingredientBenzalkonium Chloride, Benzocaine
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                     Purpose
Benzocaine USP  20%.......................................External analgesic

Benzalkonium Chloride   0.1%...........................First Aid Antiseptic

INDICATIONS & USAGE SECTION

Uses

Temporarily relieves pain and itching due to: • sunburn • minor burns • minor cuts • scrapes • insect bites • minor skin irritations• first aid to help prevent infection in minor cuts, scrapes, bites and burns

WARNINGS SECTION

Warnings
For external use only.

Flammable: Do not use while smoking or near heat or flame Do not use in large quantities, particularly over raw surfaces or blistered areas
When using this product
• keep out of eyes
• do not apply over large areas of the body or in large quantites. in case of deep or puncture wounds, animal bites, or serious burns, concult a doctor
Stop use and ask doctor if
• condition gets worse • symptoms last more than 7 days
• symptoms clear up and occur again in a few days

•do not use longer than 1 week unless directed by doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

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 SECTION

Inactive Ingredients:
Alcohol Denat.
Diisopropyl Adipate
Propylene Glycol
Tocopheryl Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2043455benzalkonium chloride 0.1 % / benzocaine 20 % Topical SprayPSN1
2043455benzalkonium chloride 1 MG/ML / benzocaine 200 MG/ML Topical SpraySCD1
2043455benzalkonium Cl 0.1 % / benzocaine 20 % Topical SpraySY1

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-7779-032020-01-31C16284748780-19d75b9d0-5146-f424-e053-dadaa90a57ceWalgreens Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-7779-03Antiseptic Pain Relieving85 g in 1 CANSPRAY851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-7779ANTISEPTIC PAIN RELIEVING (BENZALKONIUM CHLORIDE 0.10% BENZOCAINE 20.00%) SPRAY [WALGREENS]1Legacy NDC, 1 package rows20180427_3c418897-e559-4bff-a1e4-ee1ca76269f8.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-77790363-7779-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
f99f1d53-5eb8-4500-886d-7f3f6b1277543c418897-e559-4bff-a1e4-ee1ca76269f82018-04-27WarningsExact identifier
spl id: f99f1d53-5eb8-4500-886d-7f3f6b127754
spl set id: 3c418897-e559-4bff-a1e4-ee1ca76269f8

Reported adverse events (FAERS/openFDA)#

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