Home NDC 65923-532 Coralite Ultra Strength Pain Relief
Product NDC 65923-532
11-digit product format 659230532
Labeler code 65923
Product ID 65923-532_425530d6-e8ea-f05c-e063-6294a90aff39
Type HUMAN OTC DRUG
Nonproprietary name Camphor Menthol
Dosage form OINTMENT
Route TOPICAL
Labeler United Exchange Corp.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-10-15
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 110; 110 mg/g; mg/g
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 Coralite Ultra Strength Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 110 mg/g MENTHOL 110 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup 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 1089831 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 65923-532-18 Coralite Ultra Strength Pain Relief 1 in 1 CARTON OINTMENT 1 13 65923-532-18 Coralite Ultra Strength Pain Relief 18 g in 1 JAR OINTMENT 18 13
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65923-532 CORALITE ULTRA STRENGTH PAIN RELIEF (CAMPHOR MENTHOL) OINTMENT [UNITED EXCHANGE CORP.] 11 Current NDC, Legacy NDC, 2 package rows 20241222_44ecf959-cc07-4adc-a500-075b2ee69548.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 102 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pain Relief Medicated CAMPHOR MENTHOL METHYL SALICYTATE RITE AID CORPORATION 60895211-69f3-478b-a33f-1c2071f62950 2025-01-16 Warnings Exact identifier application number: M017 Elgin Pain Relief MENTHOL Eco-Logics, Inc. 70eda21e-e566-42f4-9a49-b0d3ad000652 2025-01-16 Warnings Exact identifier application number: M017 Curist Lidocaine Patch Maximum Strength LIDOCAINE Little Pharma, Inc. e574c188-cc65-287d-e053-2995a90a5972 2025-01-16 Warnings Exact identifier application number: M017 Equate Hydrocortisone Topical HYDROCORTISONE WalMart 1f64555d-f77e-4a83-b222-fdb3ed7d8853 2025-01-16 Warnings Exact identifier application number: M017 Equate Hydrocortisone HYDROCORTISONE WalMart f5c32b4a-1159-4b7a-b8ac-256d53020dc2 2025-01-16 Warnings Exact identifier application number: M017 Lidocaine Pain Relief Gel-Patch LIDOCAINE Guangzhou Zhupuyou E-commerce Co., Ltd 296fcc36-563f-19ca-e063-6394a90ab3ae 2025-01-15 Warnings Exact identifier application number: M017 K19 RELIEF MENTHOL K19 LLC e2e1ca96-1ae8-4c99-b8de-ce26754292f9 2025-01-15 Warnings Exact identifier application number: M017 Anecream LIDOCAINE 4% Focus Health Group 2d7706e2-7363-4047-96cb-85b718277e8c 2025-01-15 Warnings Exact identifier application number: M017 Boroleum CAMPHOR, MENTHOL, WHITE PETROLATUM Reliable 1 Laboratories 846568af-0fdd-a80e-e053-2a91aa0a9c9e 2025-01-15 Warnings Exact identifier application number: M017 LidoPro Pain Relief CAPSAICIN AND LIDOCAINE Advanced Rx of Tennessee, LLC 27d5997b-1cc2-41c2-e063-6394a90ac74a 2025-01-15 Warnings Exact identifier application number: M017 Pain Relief Patch 4% Lidocaine LIDOCAINE Reliable 1 Laboratories LLC 2b624763-c310-63d9-e063-6394a90a1928 2025-01-15 Warnings Exact identifier application number: M017 Cannarelief 1000mg MENTHOL Carolina Cannabis Creations LLC 01e2ae1a-c969-6dd2-e063-6394a90a9d9e 2025-01-15 Warnings Exact identifier application number: M017 Healing Hand Cream 2000mg MENTHOL Carolina Cannabis Creations LLC 01f8795b-9f95-c793-e063-6394a90a8330 2025-01-15 Warnings Exact identifier application number: M017 CBD Clinic Deep-Rub Pain Relief - Level 5 CAMPHOR, MENTHOL ABACUS HEALTH PRODUCTS, INC. 31e2e5cd-d33e-f058-e063-6394a90af7d2 2025-01-14 Warnings Exact identifier application number: M017 Meijer Odor Free Analgesic Pain Relieving Topical Analgesic LIDOCAINE HYDROCHLORIDE Meijer Distribution, Inc 6288efea-f636-4eea-bb9f-78aa2f9af54a 2025-01-14 Warnings Exact identifier application number: M017 IKONIK TONIK LIDOCAINE HYDROCHLORIDE IKONIK CARE, LLC 122fdfe8-b5fa-46d1-9fd9-3df9887ed320 2025-01-14 Warnings Exact identifier application number: M017 elp essential MANTECA DE UBRE METHYL SALICYLATE, CAMPHOR Miramar Cosmetics, Inc DBA Miramar Lab c3964dfe-17fe-4d89-a4c4-cf500f982259 2025-01-13 Warnings Exact identifier application number: M017 Methylten METHYL SALICYLATE 10% Puretek Corporation 28f4093f-803f-0e70-e063-6294a90a98a4 2025-01-13 Warnings Exact identifier application number: M017 Refill Bundle 7 Large Office BENZALKONIUM CHLORIDE CMC Group, Inc. 6620a8f3-098d-d045-e053-2a91aa0a0d94 2025-01-13 Warnings Exact identifier application number: M017 Jakwork Numbing Cream NUMBING CREAM Guangzhou Zanming Trading Co., Ltd. 2ba1de83-494a-6c54-e063-6294a90a9b2d 2025-01-13 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 Marketing end Sample Exclude flag Status 65923-532-18 65923053218 1 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR 1 jar 2017-12-13 0000-00-00 No No Current