Home NDC 66902-235 Fast Freeze Lidocaine Roll-On
Product NDC 66902-235
11-digit product format 669020235
Labeler code 66902
Product ID 66902-235_23a8a69d-a66a-47bd-e063-6394a90af015
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Hydrochloride, Benzyl Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Natural Essentials, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-07-10
Substance LIDOCAINE HYDROCHLORIDE; BENZYL ALCOHOL
Active strength 40; 10 mg/mL; mg/mL
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 Fast Freeze Lidocaine Roll-On
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 40 mg/mL BENZYL ALCOHOL 10 mg/mL
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 66902-235-03 Fast Freeze Lidocaine Roll-On 89 mL in 1 CONTAINER LIQUID 89 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66902-235 FAST FREEZE LIDOCAINE ROLL-ON (LIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOL) LIQUID [NATURAL ESSENTIALS, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20241006_74b06366-5eb4-4eba-aa2b-2b672828294d.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 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 Marketing end Sample Exclude flag Status 66902-235-03 66902023503 89 mL in 1 CONTAINER (66902-235-03) 89 ml 2020-07-10 0000-00-00 No No Current