Home NDC 69693-002 Thermacare Heat Therapy Max Strength Lidocaine Pain Relief Rollon
Product NDC 69693-002
11-digit product format 696930002
Labeler code 69693
Product ID 69693-002_4482d34d-eacb-5522-e063-6394a90a6afb
Type HUMAN OTC DRUG
Nonproprietary name Thermacare Heat Therapy Max Strength Lidocaine Pain Relief Rollon
Dosage form LIQUID
Route TOPICAL
Labeler Clarion Brands LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-15
Substance LIDOCAINE HYDROCHLORIDE; BENZYL ALCOHOL
Active strength 4; 10 g/100mL; g/100mL
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE], Pediculicide [EPC]
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 Thermacare Heat Therapy Max Strength Lidocaine Pain Relief Rollon
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 4 g/100mL BENZYL ALCOHOL 10 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup LKG8494WBH Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1943537 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 69693-002-25 Thermacare Heat Therapy Max Strength Lidocaine Pain Relief Rollon 1 mL in 1 BOTTLE LIQUID 1 1
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 8 of 156 · 3,115 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 69693-002-25 69693000225 1 mL in 1 BOTTLE (69693-002-25) 1 ml 2025-11-15 No No Current