Home FDA labels 434a76c7-1c49-2308-e063-6294a90a964b ANAL-ESE 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 ANAL-ESE
Generic name DESENSITIZER
Manufacturer Novelties by Nasswalk, Inc.
Product type HUMAN OTC DRUG
SPL set ID 03b89eed-b433-a263-e063-6294a90a675b
SPL ID 434a76c7-1c49-2308-e063-6294a90a964b
Version 3
Effective date 2025-11-10
Source export date 2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:42:27 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 · 12 matching rows.
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. Do not use near eyes. Not for prolonged use. If condition for which preparation is used causes discomfort, or if a rash or irritation should develop, discontinue use and consult a physician. For prevention of premature ejaculation.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.