Home NDC 59898-805 MUSCLE
Product NDC 59898-805
11-digit product format 598980805
Labeler code 59898
Product ID 59898-805_32475ac6-c4d4-938d-e063-6294a90a572d
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form GEL
Route TOPICAL
Labeler WATER-JEL TECHNOLOGIES
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-04-19
Substance MENTHOL
Active strength 3.5 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 2 · 62 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 MUSCLE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 3.5 g/100mL
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 808955 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59898-805 MUSCLE (MENTHOL) GEL [WATER-JEL TECHNOLOGIES] 7 Current NDC, Legacy NDC, 14 package rows 20250410_1af399af-07b0-4899-9bcc-1e244b63b1cf.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 121 of 151 · 3,010 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Boil Ease BENZOCAINE Insight Pharmaceuticals LLC bf108934-5e1a-4059-9dcf-008f52a83fab 2024-10-25 Warnings Exact identifier application number: M017 Dermarest Eczema Medicated HYDROCORTISONE Insight Pharmaceuticals LLC 0292ab62-5088-45fa-a056-70c2fcc19ef7 2024-10-25 Warnings Exact identifier application number: M017 anti itch HYDROCORTISONE Meijer, Inc. 2db7bcab-acb8-48ad-8cd1-842ff7765ed9 2024-10-23 Warnings Exact identifier application number: M017 NATUREANCE MIRACLE MENTHOL EROS GLOBAL CORP ec1a2a1f-a38d-9c59-e053-2a95a90ad268 2024-10-23 Warnings Exact identifier application number: M017 Profoot Plantar Relief Strips CAMPHOR (NATURAL), MENTHOL, METHYL SALICYLATE Rooftop Consumer Health, Inc. 65e142d8-da21-4c55-9faf-b387cb6c2c0e 2024-10-23 Warnings Exact identifier application number: M017 Profoot Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Rooftop Consumer Health, Inc. cc011b79-2761-40f7-8142-88f8e30a179a 2024-10-23 Warnings Exact identifier application number: M017 Profoot Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE Profoot, Inc. 06f82bde-41a1-35f6-e063-6394a90a6437 2024-10-23 Warnings Exact identifier application number: M017 Deep Cover Bug Bite Relief BENZOCAINE Morrisons Outdoors, LLC 25010dd6-fb48-8ee7-e063-6394a90aee6c 2024-10-21 Warnings Exact identifier application number: M017 Evel Knievels Natural Choice Pain Relief MENTHOL, UNSPECIFIED FORM Natural Essentials, Inc. 4576656c-4b6e-6965-7665-6c52756c6573 2024-10-21 Warnings Exact identifier application number: M017 berkley and jensen anti itch HYDROCORTISONE BJWC 5cc6e4f6-c62d-4923-9726-9dbc569a3f49 2024-10-19 Warnings Exact identifier application number: M017 DG Health Hydrocortisone Maximum Strength HYDROCORTISONE Dolgencorp Inc 2cc792b8-dce6-4178-bd6d-63ba268b7747 2024-10-19 Warnings Exact identifier application number: M017 Careland Hydrogel Pain Relief Patches LIDOCAINE, MENTHOL Planet (Anhui) Pharmaceutical Co., Ltd. e970070c-1c3b-49f0-8298-e6c5ebbf50a0 2024-10-18 Warnings Exact identifier application number: M017 Fruit of the Earth Cool Blue Aloe Mist Continuous LIDOCAINE HYDROCHLORIDE Fruit Of The Earth, Inc. d4caae4c-efba-2453-e053-2995a90a5e5f 2024-10-18 Warnings Exact identifier application number: M017 CVS Health Sunburn Relief Cooling Lidocaine 0.5 Pain-Relieving LIDOCAINE HCL CVS Pharmacy f0f1969d-10e0-76ee-e053-2995a90a7336 2024-10-17 Warnings Exact identifier application number: M017 Wong To Yick External Analgesic CAMPHOR MENTHOL METHYL SALICYLATE Wong To Yick Wood Lock Ointment Ltd 16a21af4-6bc0-4ae1-aa3b-1da84c8286e2 2024-10-17 Warnings Exact identifier application number: M017 Wong To Yick External Analgesic CAMPHOR MENTHOL METHYL SALICYLATE Wicsun Trading Inc 0b4bd444-b3c1-47aa-a7e3-f16c92326124 2024-10-17 Warnings Exact identifier application number: M017 Fruit of the Earth Sun Town City Aloe Vera After Sun with Lidocaine HCL LIDOCAINE Fruit of the Earth, Inc. c7a833bd-7457-73a3-e053-2a95a90ac53f 2024-10-17 Warnings Exact identifier application number: M017 Wegmans Aloe After Sun Gel with Lidocaine HCl External Analgesic LIDOCAINE HYDROCHLORIDE WEGMANS FOOD MARKETS INC f70bc438-7ed8-f74d-e053-6394a90a2b3f 2024-10-16 Warnings Exact identifier application number: M017 EQUATE Sunburn relief with Aloe After Sun LIDOCAINE Wal-Mart Stores Inc c25e1288-7ac6-41fc-ab65-26c379f288a7 2024-10-16 Warnings Exact identifier application number: M017 Genuine First Aid Insect Sting Relief Pad 1 ct BENZOCAINE, ALCOHOL GFA Production (Xiamen) Co., Ltd. b119ba37-0ee1-851a-e053-2995a90a85b1 2024-10-15 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 59898-805-05 59898080505 96 PACKET in 1 BOX, UNIT-DOSE (59898-805-05) / 3.8 mL in 1 PACKET 96 packet 2010-04-19 0000-00-00 No No Current 59898-805-10 59898080510 59 mL in 1 BOTTLE, SPRAY (59898-805-10) 59 ml 2013-03-17 0000-00-00 No No Current 59898-805-17 59898080517 1728 PACKET in 1 CARTON (59898-805-17) / 3.8 mL in 1 PACKET 1728 packet 2010-04-19 0000-00-00 No No Current 59898-805-18 59898080518 5 PACKET in 1 BOX, UNIT-DOSE (59898-805-18) / 3.8 mL in 1 PACKET 5 packet 2010-04-19 0000-00-00 No No Current 59898-805-20 59898080520 24 PACKET in 1 CARTON (59898-805-20) / 3.8 mL in 1 PACKET 24 packet 2010-04-19 0000-00-00 No No Current 59898-805-21 59898080521 473 mL in 1 BOTTLE, PUMP (59898-805-21) 473 ml 2010-04-19 0000-00-00 No No Current 59898-805-22 59898080522 80 mL in 1 BOTTLE, DISPENSING (59898-805-22) 80 ml 2010-04-19 0000-00-00 No No Current 59898-805-23 59898080523 946 mL in 1 BOTTLE, PUMP (59898-805-23) 946 ml 2010-04-19 0000-00-00 No No Current 59898-805-24 59898080524 3784 mL in 1 BOTTLE, PUMP (59898-805-24) 3784 ml 2010-04-19 0000-00-00 No No Current 59898-805-25 59898080525 118 mL in 1 TUBE (59898-805-25) 118 ml 2010-04-19 0000-00-00 No No Current