Home NDC 83559-018 ENOKON PAIN RELIEF Spray.
Product NDC 83559-018
11-digit product format 835590018
Labeler code 83559
Product ID 83559-018_5675ec21-b948-2206-e063-6294a90aa509
Type HUMAN OTC DRUG
Nonproprietary name PAIN RELIEF Spray.
Dosage form SPRAY
Route TOPICAL
Labeler Henan Enokon Medical Instrument Co., Ltd.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-13
Substance LIDOCAINE
Active strength 4 g/100mL
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base ENOKON PAIN RELIEF Spray.
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1869797 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83559-018-01 83559001801 30 mL in 1 BOX (83559-018-01) 30 ml 2026-07-13 No No Current 83559-018-02 83559001802 50 mL in 1 BOX (83559-018-02) 50 ml 2026-07-13 No No Current