Home NDC 13709-360 Lidocaine Pain Relief Roll on
Product NDC 13709-360
11-digit product format 137090360
Labeler code 13709
Product ID 13709-360_58ff9d2d-99e7-8f98-e063-6394a90a8de7
Type HUMAN OTC DRUG
Nonproprietary name Pain Relief Roll on
Dosage form LIQUID
Route TOPICAL
Labeler NeilMed Pharmaceuticals Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-17
Substance LIDOCAINE
Active strength 3.4 g/85g
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 Lidocaine Pain Relief Roll on
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 3.4 g/85g
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 2197844 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 109 of 152 · 3,029 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 13709-360-01 13709036001 1 BOTTLE, WITH APPLICATOR in 1 CARTON (13709-360-01) / 85 g in 1 BOTTLE, WITH APPLICATOR 2026-08-17 No No Current