FDA.reportPublic FDA data

LubeLife Climax Control Delay

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
LubeLife Climax Control Delay
Generic name
BENZOCAINE
Manufacturer
CC Wellness LLC
Product type
HUMAN OTC DRUG
SPL set ID
e1a98e6d-0c24-75b8-e053-2a95a90ad136
SPL ID
3e62265a-9563-8fee-e063-6394a90a13d4
Version
3
Effective date
2025-09-09
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 06:26:06
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 · 4 matching rows.

warnings

For external use only Avoid contact with the eyes Allergy alert: do not use this product if you are allergic (sensitive) to local anesthetics or any of the other listed ingredients Do not use on broken or inflamed skin Ask a doctor before use: If your partner is pregnant If you have or have had liver or kidney problems

warnings

Avoid contact with the eyes

warnings

Allergy alert: do not use this product if you are allergic (sensitive) to local anesthetics or any of the other listed ingredients

warnings

Do not use on broken or inflamed skin

Reported adverse events (FAERS/openFDA)#

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