Home NDC 51452-450 POINT RELIEF COLD SPOT Pain Relieving
Product NDC 51452-450
11-digit product format 514520450
Labeler code 51452
Product ID 51452-450_10c7bc76-f8e5-858c-e063-6294a90a0c13
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form GEL
Route TOPICAL
Labeler FABRICATION ENTERPRISES
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-26
Substance MENTHOL
Active strength 120 mg/mL
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 POINT RELIEF COLD SPOT Pain Relieving
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 120 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2121666 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51452-450-01 POINT RELIEF COLD SPOT Pain Relieving 3800 mL in 1 JUG GEL 3800 1 51452-450-16 POINT RELIEF COLD SPOT Pain Relieving 475 mL in 1 JUG GEL 475 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51452-450 POINT RELIEF COLD SPOT PAIN RELIEVING (MENTHOL) GEL [FABRICATION ENTERPRISES] 1 Current NDC, 2 package rows 20240226_96f1d592-6cec-412e-a5fd-cf3c4f68644f.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 125 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join DermacinRx Penetral Cream CAPSAICIN PureTek Corporation 1e343a52-6071-3230-e054-00144ff8d46c 2024-10-02 Warnings Exact identifier application number: M017 Eagle Medicated Aromatic CAMPHOR MENTHOL METHYL SALICYLATE Borden Company (Private) Limited 36abfc2c-d424-4df8-968d-866342c96a56 2024-10-02 Warnings Exact identifier application number: M017 Eagle Balm CAMPHOR MENTHOL Eagle Indo Pharma, PT 87614869-9675-2c76-e053-2a95a90a48a9 2024-10-02 Warnings Exact identifier application number: M017 Eagle Medicated MENTHOL METHYL SALICYLATE Borden Company (Private) Limited d9a93daa-4e24-6690-e053-2a95a90a147c 2024-10-02 Warnings Exact identifier application number: M017 Eagle Extra Strength MENTHOL METHYL SALICYLATE Borden Company (Private) Limited 5e02fbe3-5bc7-430e-b661-3a760ddd8fe0 2024-10-02 Warnings Exact identifier application number: M017 Eagle Medicated Oil Refreshing MENTHOL, METHYL SALICYLATE Borden Company (Private) Limited c62a4313-2c07-5f58-e053-2995a90a083a 2024-10-02 Warnings Exact identifier application number: M017 Eagle Medicated Aromatic CAMPHOR MENTHOL METHYL SALICYLATE Eagle Indo Pharma, PT e272ec90-3cd9-5b70-e053-2a95a90a1df4 2024-10-02 Warnings Exact identifier application number: M017 RUGBY HYDROCORTISONE WITH ALOE HYDROCORTISONE A-S Medication Solutions b2674075-aaa4-4c77-bcaa-a76336b3c321 2024-10-02 Warnings Exact identifier application number: M017 Herb Street Anti-Itch Stick HYDROCORTISONE Balassa Laboratories Inc. 8717faae-59c3-4c6f-9ef1-285c0d2445ed 2024-10-01 Warnings Exact identifier application number: M017 Herb Street Backache and Sore Muscle Relief MENTHOL Balassa Laboratories Inc. aeac1b64-8689-4b3d-a41c-db41061257b5 2024-10-01 Warnings Exact identifier application number: M017 Herb Street Arthritis Relief MENTHOL/CAMPHOR Balassa Laboratories Inc. a9d8ceb7-def0-415f-8fc1-ff8dd3e41855 2024-10-01 Warnings Exact identifier application number: M017 Lido King Lidocaine 4% Pain Relieving Gel-Patch LIDOCAINE Galaxy Bio, Inc. 2243734a-4ea2-a5e5-e063-6294a90aba15 2024-10-01 Warnings Exact identifier application number: M017 Medicated Herbal Lip Balm MENTHOL Earth Mama Angel Baby LLC 1cc2391e-6a7a-609c-e063-6394a90a6305 2024-10-01 Warnings Exact identifier application number: M017 CVS Health Lidocaine Plus Pain Relieving LIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOL NATURAL ESSENTIALS, INC. 1adb9b74-4a01-4461-b845-f3aedcb3f810 2024-10-01 Warnings Exact identifier application number: M017 Circata CAPSAICIN PureTek Corporation b67161d7-cc5c-e971-e053-2995a90acbe7 2024-10-01 Warnings Exact identifier application number: M017 Menticam CAMPHOR,MENTHOL, METHYL SALICYLATE PureTek Corporation ffea2e97-777f-434b-e053-6394a90a3a63 2024-10-01 Warnings Exact identifier application number: M017 Herb Street Sore Muscle Relief METHYL SALICYLATE Balassa Laboratories Inc. e43943c2-d4cd-44c5-a0ff-403a8d42860f 2024-10-01 Warnings Exact identifier application number: M017 hydrocortisone HYDROCORTISONE Kroger Company 68dab606-0385-48b7-9a7b-a2cf83d20393 2024-09-29 Warnings Exact identifier application number: M017 kirkland signature hydrocortisone plus maximum strength HYDROCORTISONE Costco Wholesale Company 481341c5-db1f-43fb-aed7-f40495a4eab8 2024-09-29 Warnings Exact identifier application number: M017 Care One hydrocortisone maximum strength HYDROCORTISONE American Sales Company 32593229-d0ac-4d6c-831a-089fc6e76152 2024-09-29 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 51452-450-01 51452045001 3800 mL in 1 JUG (51452-450-01) 3800 ml 2024-02-26 No No Current 51452-450-16 51452045016 475 mL in 1 JUG (51452-450-16) 475 ml 2024-02-26 No No Current