Home NDC 68678-040 Pain Relieving Roll-On
Product NDC 68678-040
11-digit product format 686780040
Labeler code 68678
Product ID 68678-040_3dd5fc5a-32c4-78bf-e063-6394a90af02a
Type HUMAN OTC DRUG
Nonproprietary name Menthol, Camphor, Capsaicin
Dosage form LOTION
Route TOPICAL
Labeler AHC VENTURES CORP DBA CRY
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-01-01
Substance MENTHOL; CAMPHOR (SYNTHETIC); CAPSAICIN
Active strength 3.85; 3.85; .0355 g/100mL; g/100mL; 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 1 · 40 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 68678-040-90 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 68678-040-90 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 68678-040-90 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 68678-040-90 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 68678-040-90 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 68678-040-90 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 68678-040-90 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 68678-040-90 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 68678-040-90 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 68678-040-90 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 68678-040-90 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 68678-040-90 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 68678-040-90 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 68678-040-90 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 68678-040-90 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 68678-040-90 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 68678-040-90 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 68678-040-90 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 68678-040-90 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 68678-040-90 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
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 Pain Relieving Roll-On
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 3.85 g/100mL CAMPHOR (SYNTHETIC) 3.85 g/100mL CAPSAICIN .0355 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 5TJD82A1ET Internal UNII lookup S07O44R1ZM Internal UNII 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 68678-040-90 Pain Relieving Roll-On 84 mL in 1 BOTTLE, DISPENSING LOTION 84 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68678-040 PAIN RELIEVING ROLL-ON (MENTHOL, CAMPHOR, CAPSAICIN) LOTION [AHC VENTURES CORP DBA CRY] 3 Current NDC, Legacy NDC, 1 package rows 20220422_799751f3-726a-42de-934e-dbc3cd1cb8b8.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 37 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join PAIN RELIEF PATCHES LIDOCAINE WALMART STORES INC b82cfe42-f521-4784-8c60-98481524c5ec 2026-01-29 Warnings Exact identifier application number: M017 Equate Pain Relief Patch Camphor/Menthol/Salicylate CAMPHOR, MENTHOL, METHYL SALICYLATE Walmart Stores Inc b869848c-21e2-5ca2-e053-2995a90a86f2 2026-01-29 Warnings Exact identifier application number: M017 HEATING PAIN RELIEF METHYL SALICYLATE, MENTHOL SUNSET NOVELTIES, INC 498cd2aa-ee59-67b5-e063-6294a90ac242 2026-01-29 Warnings Exact identifier application number: M017 COOLING PAIN RELIEF MENTHOL, CAMPHOR SUNSET NOVELTIES, INC 498d76d8-788b-4cc7-e063-6294a90a1696 2026-01-29 Warnings Exact identifier application number: M017 MQUPIN Lidocaine Gel-Patch LIDOCAINE GEL-PATCH Zhengzhou Miaoqi Medical Technology Co., Ltd. 49703717-69a6-e480-e063-6394a90ac69c 2026-01-28 Warnings Exact identifier application number: M017 MQXUNMI LIDOCAINE Pain Relief Patch LIDOCAINE PAIN RELIEF PATCH Zhengzhou Miaoqi Medical Technology Co., Ltd. 49706db7-bacd-190f-e063-6394a90a3a8e 2026-01-28 Warnings Exact identifier application number: M017 Joint and Muscle Relief Topical Analgesic MENTHOL Smart Cookie Solutions 1ecf56b1-ffcb-486f-9fdd-d4dc92aefc1d 2026-01-28 Warnings Exact identifier application number: M017 VonaFlex Effective Pain Relief Topical Analgesic LIDOCAINE HYDROCHLORIDE OPTIMAL LABORATORIES, LLC 0901244a-7d41-413a-b424-92a807532f28 2026-01-28 Warnings Exact identifier application number: M017 Lidocaine Pain Relief Gel Patch LIDOCAINE PAIN RELIEF Dynarex 960e4240-cd09-2560-e053-2a95a90a7bcf 2026-01-28 Warnings Exact identifier application number: M017 ALOE ICE SUNBURN RELIEF LIDOCAINE HYDROCHLORIDE Aloe Care International, LLC 56866fa8-052e-497c-a954-978d7d628949 2026-01-28 Warnings Exact identifier application number: M017 Walgreens Original Strength Anti Itch DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE Walgreen Company a6a49dbb-74c7-47ca-88f2-3bb3d9acf914 2026-01-28 Warnings Exact identifier application number: M017 Flobow QUIT SMOKING Nicotine NICOTINE18% MENTHOL 0.3% QUIT SMOKING NICOTINE Jiangxi Yudexi Pharmaceutical Co., LTD 495b10ce-3d2d-1aa4-e063-6294a90a4f35 2026-01-27 Warnings Exact identifier application number: M017 PAIN REUSEABLE PAIN Shenzhen Mengyue Technology Co., Ltd. 44e058fc-e1c0-742b-e063-6294a90ad225 2026-01-27 Warnings Exact identifier application number: M017 HealthWise Pain Relieving Cream Lavender MENTHOL Veridian Healthcare 495eb6e9-69da-f7b6-e063-6294a90accee 2026-01-27 Warnings Exact identifier application number: M017 HealthWise Pain Relieving Cream MENTHOL Veridian Healthcare 49548ab2-267e-1e2a-e063-6394a90ab391 2026-01-27 Warnings Exact identifier application number: M017 Itch Relief DIPHENHYDRAMINE HCL Wal-Mart Stores, Inc. 03feaaef-7401-d464-e063-6294a90a2b2d 2026-01-27 Warnings Exact identifier application number: M017 Hydrocortisone with Aloe HYDROCORTISONE STRATEGIC SOURCING SERVICES LLC 4a113699-1eb7-49b8-8cdf-2ad57db89b81 2026-01-27 Warnings Exact identifier application number: M017 Healthy Back Institute Rub On Relief ANALGESIC Fullstack Fulfillment 284c29a3-5722-ce70-e063-6394a90a7fa0 2026-01-26 Warnings Exact identifier application number: M017 Velocx for Joint and Muscle Pain Roll-On Applicator MENTHOL, METHYL SALICYLATE JMAD Consulting LLC, dba JMAD Labs dbf3eaa3-d85e-46b1-b4a5-a87ba4dc5d21 2026-01-26 Warnings Exact identifier application number: M017 CAPSAICIN HEAT PATCHES BACK AND LARGE AREAS CAPSAICIN Meijer Distribution Inc 9b91658f-c15f-4222-bbd9-881b29de3b6e 2026-01-26 Warnings Exact identifier application number: M017
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68678-040-90 68678004090 84 mL in 1 BOTTLE, DISPENSING (68678-040-90) 84 ml 2016-01-01 0000-00-00 No No Current