Roman Swipes

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: Roman Swipes
Generic name: BENZOCAINE
Manufacturer: Roman Health Ventures Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 7f0eac8c-7235-99d8-e053-2a91aa0a634e
SPL ID: 2df3ab8d-6918-a250-e063-6294a90a64f9
Version: 8
Effective date: 2025-02-12
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:01

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Roman Swipes	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		Roman Health Ventures Inc.	openfda.manufacturer_name
ndc	package	72484-433-08	openfda.package_ndc
ndc	package	72484-433-12	openfda.package_ndc
ndc	package	72484-433-02	openfda.package_ndc
ndc	package	72484-433-05	openfda.package_ndc
ndc	package	72484-433-03	openfda.package_ndc
ndc	product	72484-433	openfda.product_ndc
ndc11	package	72484043305	derived:openfda.package_ndc
ndc11	package	72484043308	derived:openfda.package_ndc
ndc11	package	72484043312	derived:openfda.package_ndc
ndc11	package	72484043302	derived:openfda.package_ndc
ndc11	package	72484043303	derived:openfda.package_ndc
spl id		2df3ab8d-6918-a250-e063-6294a90a64f9	id
spl set id		7f0eac8c-7235-99d8-e053-2a91aa0a634e	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 When using this product avoid contact with the eyes. Stop use and ask a doctor if this product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision. you or your partner develop a rash or irritation, such as burning or itching symptoms persist. 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.