Home NDC 36800-290 TopCare Pain Relieving Roll-On
Product NDC 36800-290
11-digit product format 368000290
Labeler code 36800
Product ID 36800-290_d6e69347-6255-4460-97e1-754359314327
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, UNSPECIFIED FORM
Dosage form GEL
Route TOPICAL
Labeler Topco Associates LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-03
Substance MENTHOL, UNSPECIFIED FORM
Active strength 40 mg/mL
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 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 36800-290-01 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 36800-290-01 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 36800-290-01 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 36800-290-01 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 36800-290-01 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 36800-290-01 1332a3947898…d4bfe170f9cd…
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 TopCare Pain Relieving Roll-On
Brand name suffix Topical Analgesic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 40 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 415974 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 36800-290-01 TopCare Pain Relieving Roll-OnTopical Analgesic 74 mL in 1 BOTTLE, WITH APPLICATOR GEL 74 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 36800-290 TOPCARE PAIN RELIEVING ROLL-ON TOPICAL ANALGESIC (MENTHOL, UNSPECIFIED FORM) GEL [TOPCO ASSOCIATES LLC] 3 Current NDC, Legacy NDC, 1 package rows 20241115_48589893-ca67-471d-88bc-92014295ab9f.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 149 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SCLERA CARE Topical Anesthetic Gel LIDOCAINE HYDROCHLORIDE ScleraCare, LLC 488ace02-fc0b-4d13-ab89-0e1640e915e5 2023-11-05 Warnings Exact identifier application number: M017 IRELIEV ROLL ON COOL PAIN RELIEF MENTHOL Excel Health, Inc dab94995-7393-4d9c-b295-72611a90919b 2023-11-05 Warnings Exact identifier application number: M017 URIFLEX Fast Acting Analgesic Pain Relief MENTHOL Rejuvica LLC fb78f705-b838-461d-b42c-8c98d3ca5d09 2023-11-05 Warnings Exact identifier application number: M017 365 Medicated Lip Balm MEDICATED LIP BALM Whole Foods Market, Inc. 48309a7d-d2da-483c-8bf8-f59d9ad0bb73 2023-11-03 Warnings Exact identifier application number: M017 COOL BREEZE Pain Relief MENTHOL COOL BREEZE US LLC 14dcf4ee-6778-49d4-8601-9205737432ea 2023-11-01 Warnings Exact identifier application number: M017 Lidozen LIDOCAINE HYDROCHLORIDE, MENTHOL Proficient Rx LP 1ebb45e5-4541-4c95-abe1-661ef763a610 2023-11-01 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Cream LIDOCAINE 4% Walgreens ce1b55ed-f5c5-ea8b-e053-2a95a90acd40 2023-10-31 Warnings Exact identifier application number: M017 Walgreens pain relieving LIDOCAINE 4% Walgreens ce2b9e57-749d-715c-e053-2995a90aaf8d 2023-10-31 Warnings Exact identifier application number: M017 Walgreens Cool n heat LIDOCAINE 4% MENTHOL 1% Walgreens ce168ab7-ec4a-daea-e053-2995a90af829 2023-10-31 Warnings Exact identifier application number: M017 Methyl Salicylate 40 Percent METHYL SALICYLATE Alexso, Inc 53407aab-094c-4393-a2b9-54fd85321e3e 2023-10-31 Warnings Exact identifier application number: M017 Hydrocortisone Acetate HYDROCORTISONE ACETATE Bentlin Products LLC 4346351c-8e11-46ae-b428-98d17f55beb9 2023-10-30 Warnings Exact identifier application number: M017 Biofreeze Roll-On MENTHOL A-S Medication Solutions 814b37ea-5441-4cec-8794-71ca01d849ae 2023-10-30 Warnings Exact identifier application number: M017 Dr. Sheffield Hydrocortisone Anti itch HYDROCORTISONE Sheffield Pharmaceuticals LLC 71c9f2f4-2188-45eb-b55e-3856ac78070b 2023-10-30 Warnings Exact identifier application number: M017 Family Wellness BENZOCAINE, RESORCINOL Zhejiang Jingwei Pharmaceutic Al Co., Ltd. df540eb8-6773-4647-9cc2-c3fd14d7355e 2023-10-27 Warnings Exact identifier application number: M017 Family Wellness HYDROCORTISONE 1% FRONT PHARMACEUTICAL PLC ea26265d-f24e-458e-8bf0-287b2d49f4f4 2023-10-27 Warnings Exact identifier application number: M017 Joint Formula 88 MAX PLUS CAMPHOR Sarati International, Inc. f5d78335-b78d-4909-a88b-9daa3c18ba15 2023-10-27 Warnings Exact identifier application number: M017 OsmoFlex MENTHOL Sarati International, Inc. 479147c0-4cf4-4d7a-8b8e-1a0de49ed73e 2023-10-27 Warnings Exact identifier application number: M017 Thera plus Anti-itch with aloe Hydrocortisone HYDROCORTISONE Fourstar Group USA, Inc. c69d0670-a65b-1680-e053-2995a90a2ee5 2023-10-26 Warnings Exact identifier application number: M017 Family Wellness DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE FRONT PHARMACEUTICAL PLC fde2069b-344e-46da-bb95-c5113e0f35d6 2023-10-26 Warnings Exact identifier application number: M017 MAXIMUM STRENGTH HEMORRHOIDAL RELIEF LIDOCAINE CVS PHARMACY, INC b61424bf-3b23-420b-a7bc-256ddb96aa22 2023-10-25 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 36800-290-01 36800029001 74 mL in 1 BOTTLE, WITH APPLICATOR (36800-290-01) 74 ml 2020-09-03 0000-00-00 No No Current