Promescent

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
Promescent
Generic name
LIDICAINE
Manufacturer
Absorption
Product type
HUMAN OTC DRUG
SPL set ID
5b508238-3be7-4b0d-bf35-51de79f58f55
SPL ID
5578bdd9-b03b-b909-e063-6294a90a0c79
Version
12
Effective date
2026-06-30
Source export date
2026-11-06
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/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:26:08
Harmonized routes table
Harmonized routes
TOPICAL

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 if ​ You or your partner are allergic to lidocaine or topical anesthetics. Your partner is, or may be pregnant. ​Ask a doctor or pharmacist before use if ​ You have liver problems. ​When using this product ​ Do not spray on broken, irritated or sensitive skin. Avoid contact with the eyes. ​Stop use and ask a doctor If you or your partner develop a rash or irritation, such as burning or itching, dicontinue use. If symptoms persist, consult a doctor. Premature ejaculation may be due to a condition requiring medical supervision. If this product, used as directed does not provide relief, discontinue use and consult a doctor. ​​

Reported adverse events (FAERS/openFDA)#

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