Sting and Bite

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: Sting and Bite
Generic name: BENZOCAINE
Manufacturer: PHOENIX HEALTHCARE SOLUTIONS, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 82791832-1357-48ca-91d4-132899701261
SPL ID: 41d33c47-0f90-63eb-e063-6294a90a5874
Version: 13
Effective date: 2025-10-23
Source export date: 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:51

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Sting and Bite	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		PHOENIX HEALTHCARE SOLUTIONS, LLC	openfda.manufacturer_name
ndc	package	60913-031-01	openfda.package_ndc
ndc	product	60913-031	openfda.product_ndc
ndc11	package	60913003101	derived:openfda.package_ndc
rxcui		1043353	openfda.rxcui
spl id		41d33c47-0f90-63eb-e063-6294a90a5874	id
spl set id		82791832-1357-48ca-91d4-132899701261	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 For external use only. Flammable, keep away from fire or flame Avoid contact with eyes; if this happens, rinse thoroughly with water Do Not Use With electrocautery procedures. Stop Use If irritation and redness develop.If condition worsens or if symptoms persist for more than 7 days, or clear up and occur again within a few days,discontinue use and consult a doctor. Caution: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.