Medi-First Sting 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: Medi-First Sting Relief
Generic name: BENZOCAINE 6%, ISOPROPYL ALCOHOL 60%
Manufacturer: Unifirst First Aid Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 6e610821-b030-930b-e053-2a91aa0a66f9
SPL ID: 3e4cef3b-1393-fc54-e063-6294a90ad5f2
Version: 7
Effective date: 2025-09-08
Source export date: 2026-10-22
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-22/54e9c48e60446f01ef435f186a51c63f4eb19a752379c30779f6422194b8316c/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
Import run: 20261023T001338Z
Imported at: 2026-10-23 00:52:08

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Medi-First Sting Relief	openfda.brand_name
generic name		BENZOCAINE 6%, ISOPROPYL ALCOHOL 60%	openfda.generic_name
manufacturer name		Unifirst First Aid Corporation	openfda.manufacturer_name
ndc	package	47682-234-12	openfda.package_ndc
ndc	package	47682-234-99	openfda.package_ndc
ndc	product	47682-234	openfda.product_ndc
ndc11	package	47682023499	derived:openfda.package_ndc
ndc11	package	47682023412	derived:openfda.package_ndc
rxcui		895749	openfda.rxcui
spl id		3e4cef3b-1393-fc54-e063-6294a90ad5f2	id
spl set id		6e610821-b030-930b-e053-2a91aa0a66f9	set_id
unii		U3RSY48JW5	openfda.unii
unii		ND2M416302	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 For external use only. Flammable, keep away from fire or flame. Do not use in the eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation, redness or other symptoms develop the condition persists or gets worse

Reported adverse events (FAERS/openFDA)#

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