7 Select Oral Pain Maximum Strength 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: 7 Select Oral Pain Maximum Strength Relief
Generic name: BENZOCAINE
Manufacturer: 7-ELEVEN, INC.
Product type: HUMAN OTC DRUG
SPL set ID: f170a570-1c50-4b9a-be16-9b01bf5eaa74
SPL ID: 427bbea1-432f-6911-e063-6394a90a9d10
Version: 9
Effective date: 2025-10-31
Source export date: 2026-10-12
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:45:01

Harmonized routes table
Harmonized routes
TOPICAL

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		M022	openfda.application_number
brand name		7 Select Oral Pain Maximum Strength Relief	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		7-ELEVEN, INC.	openfda.manufacturer_name
ndc	package	10202-853-14	openfda.package_ndc
ndc	product	10202-853	openfda.product_ndc
ndc11	package	10202085314	derived:openfda.package_ndc
rxcui		238910	openfda.rxcui
spl id		427bbea1-432f-6911-e063-6394a90a9d10	id
spl set id		f170a570-1c50-4b9a-be16-9b01bf5eaa74	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 Methemoglobinemia warning: Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate meddical attention if you or a child in your care develops: pale, gray, or blue colored skin (cyanosis) headache rapid heart rate shortness of breath dizziness or lightheadedness fatigue or lack of energy 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

Reported adverse events (FAERS/openFDA)#

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