First Aid Only Sting Relief Pad

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: First Aid Only Sting Relief Pad
Generic name: BENZOCAINE, ISOPROPYL ALCOHOL
Manufacturer: Acme United Corporation
Product type: HUMAN OTC DRUG
SPL set ID: d71047f6-1353-c758-e053-2995a90a962c
SPL ID: 27d78c3c-0918-1ac6-e063-6394a90a1d83
Version: 2
Effective date: 2024-11-26
Source export date: 2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:03:51

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		First Aid Only Sting Relief Pad	openfda.brand_name
generic name		BENZOCAINE, ISOPROPYL ALCOHOL	openfda.generic_name
manufacturer name		Acme United Corporation	openfda.manufacturer_name
ndc	package	0924-5204-02	openfda.package_ndc
ndc	package	0924-5204-03	openfda.package_ndc
ndc	package	0924-5204-05	openfda.package_ndc
ndc	package	0924-5204-01	openfda.package_ndc
ndc	package	0924-5204-04	openfda.package_ndc
ndc	product	0924-5204	openfda.product_ndc
ndc11	package	00924520401	derived:openfda.package_ndc
ndc11	package	00924520403	derived:openfda.package_ndc
ndc11	package	00924520404	derived:openfda.package_ndc
ndc11	package	00924520402	derived:openfda.package_ndc
ndc11	package	00924520405	derived:openfda.package_ndc
rxcui		895749	openfda.rxcui
spl id		27d78c3c-0918-1ac6-e063-6394a90a1d83	id
spl set id		d71047f6-1353-c758-e053-2995a90a962c	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 eyes, if contact occurs flush with water ▪over large areas of the body Consult a doctor ▪if condition worsens ▪if symptoms last for more than seven days or clear up and occur again ▪for deep puncture wounds Keep out of reach of children. If swallowed, 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.