Walgreens Pain Relief

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Walgreens Pain Relief
Generic name: BENZOCAINE
Manufacturer: Walgreens Company
Product type: HUMAN OTC DRUG
SPL set ID: 7cee7234-32cd-4bf3-8a6c-0882585eec7f
SPL ID: b305fced-9c43-464a-b813-2fc790d0df1c
Version: 2
Effective date: 2024-11-20
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:41:07

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Walgreens Pain Relief	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		Walgreens Company	openfda.manufacturer_name
ndc	package	0363-5061-33	openfda.package_ndc
ndc	product	0363-5061	openfda.product_ndc
ndc11	package	00363506133	derived:openfda.package_ndc
rxcui		238910	openfda.rxcui
spl id		b305fced-9c43-464a-b813-2fc790d0df1c	id
spl set id		7cee7234-32cd-4bf3-8a6c-0882585eec7f	set_id
unii		U3RSY48JW5	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Allergy alert: Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics. Do not use more than directed for more than 7 days unless told to do so by a dentist or doctor Stop use and ask a doctor if swelling, rash or fever develops irritation, pain, or redness persists or worsens Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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