Benzocaine

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: Benzocaine
Generic name: BENZOCAINE
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 6161e94c-7849-466e-8da3-a6f1b085bdf9
SPL ID: 47be2d03-5dbc-7930-e063-6294a90a4395
Version: 22
Effective date: 2026-01-06
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:06

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Benzocaine	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-246-04	openfda.package_ndc
ndc	package	67777-246-01	openfda.package_ndc
ndc	package	67777-246-03	openfda.package_ndc
ndc	package	67777-246-02	openfda.package_ndc
ndc	product	67777-246	openfda.product_ndc
ndc11	package	67777024604	derived:openfda.package_ndc
ndc11	package	67777024601	derived:openfda.package_ndc
ndc11	package	67777024603	derived:openfda.package_ndc
ndc11	package	67777024602	derived:openfda.package_ndc
rxcui		895749	openfda.rxcui
spl id		47be2d03-5dbc-7930-e063-6294a90a4395	id
spl set id		6161e94c-7849-466e-8da3-a6f1b085bdf9	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 • Avoid contact with eyes; if this occures, rinse thoroughly with water • Do not use with electrocautery procedures Stop use if • Irritation and redness develop • Condition worsens or symptoms persists for more than 7 days, or clear up and occur again within a few days, discontinue use and consult a doctor Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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