Home NDC 69396-120 Pain Itch Relief
Product NDC 69396-120
11-digit product format 693960120
Labeler code 69396
Product ID 69396-120_29b3acd1-d36c-c0b4-e063-6394a90a5234
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine HCI
Dosage form CREAM
Route TOPICAL
Labeler Trifecta Pharmaceutical USA LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-01-06
Substance LIDOCAINE HYDROCHLORIDE
Active strength 4 g/100g
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2026-12-31
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 Pain Itch Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 4 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1010895 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69396-120-17 Pain Itch Relief 49.6 g in 1 BOTTLE CREAM 49.6 2 69396-120-17 Pain Itch Relief 1 in 1 BOX CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69396-120 PAIN ITCH RELIEF (LIDOCAINE HCI) CREAM [TRIFECTA PHARMACEUTICAL USA LLC] 2 Current NDC, 2 package rows 20241222_f40b19a8-795c-f514-e053-2a95a90a6d15.zip
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 109 of 151 · 3,020 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69396-120-17 69396012017 1 BOTTLE in 1 BOX (69396-120-17) / 49.6 g in 1 BOTTLE 1 bottle 2023-01-06 No No Current