Home NDC 72927-976 Jointflex
Product NDC 72927-976
11-digit product format 729270976
Labeler code 72927
Product ID 72927-976_b73f0031-d9c9-42f4-b5e8-645dda4d43ac
Type HUMAN OTC DRUG
Nonproprietary name Camphor
Dosage form CREAM
Route TOPICAL
Labeler Strides Consumer LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-06-01
Substance CAMPHOR (SYNTHETIC)
Active strength 3.2 g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# Observed captured status history: Rows come only from successfully parsed FDA auxiliary ZIP captures. They show the state present in that artifact, not a continuous regulatory timeline. Absence before, after, or between captures is not proof of status, and a known non-data HTTP 403 capture is preserved in backfill provenance but cannot produce a status row.
Historic NDC status page 1 of 1 · 4 matching rows.
Browse every current auxiliary row. · Browse the complete NDC auxiliary source catalog.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product 72927-976 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 72927-976 72927-976-02 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 72927-976 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 72927-976 72927-976-02 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 153 · 3,056 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Icy Hot Original Nighttime Recovery Pain Relief No Mess Roll On MENTHOL Chattem, Inc. aa40c907-eeb5-4fda-b35e-439cbecc178c 2026-07-31 Warnings Exact identifier application number: M017 Aspercreme with Lidocaine Dry LIDOCAINE Chattem, Inc. 008abaaa-5e12-4246-a7f5-66f3966acf28 2026-07-30 Warnings Exact identifier application number: M017 Icy Hot Performance No-Mess Pain Relief Cream MENTHOL 16%, CAMPHOR 11% Chattem, Inc. 5e3e272a-c001-4f57-9535-521ccc85ae65 2026-07-30 Warnings Exact identifier application number: M017 Auixudin Lidocaine Pain Relief Gel-Patch LIDOCAINE PAIN RELIEF GEL-PATCH Henan Enokon Medical Instrument Co., Ltd. 57bc7b9e-e2f7-724b-e063-6394a90ab36f 2026-07-29 Warnings Exact identifier application number: M017 Jinfahe Lidocaine Pain Relief Patch LIDOCAINE PAIN RELIEF PATCH Henan Enokon Medical Instrument Co., Ltd. 57bcd9c5-767e-b634-e063-6394a90a2878 2026-07-29 Warnings Exact identifier application number: M017 Maximun Strength Lidocaine Patch Plus Menthol LIDOCAINE, MENTHOL Meijer Distribution Inc d0468514-58ea-4d8f-b634-a65bf95c0316 2026-07-29 Warnings Exact identifier application number: M017 Oudetas Lidocaine Cream LIDOCAINE CREAM Guangzhou Jingliang Cosmetics Co., Ltd. 57ca9220-2778-790a-e063-6294a90af506 2026-07-29 Warnings Exact identifier application number: M017 Aspercreme Lidocaine No-Mess plus Lavender LIDOCAINE HCL Chattem, Inc. 3948a3d2-ce04-4703-8709-211e75c9c38d 2026-07-29 Warnings Exact identifier application number: M017 LidoPro LIDOCAINE AND MENTHOL Clinic Pharma cdfd6b39-b430-4e95-a0f7-682cf3d78b52 2026-07-28 Warnings Exact identifier application number: M017 LidoPro Patch (Lidocaine 4%, Menthol 1%) LIDOCAINE AND MENTHOL PATCH Clinic Pharma 2b4d2105-b7ad-2695-e063-6394a90a999b 2026-07-28 Warnings Exact identifier application number: M017 Earths Care Pain Relieving CAMPHOR, MENTHOL, METHYL SALICYLATE DLC Laboratories, Inc. 5c3976da-a6cb-4b94-ae41-3e86b1ab13cb 2026-07-28 Warnings Exact identifier application number: M017 Muscle Rub Cream MENTHOL 10%, METHYL SALICYLATE 15% Preferred Pharmaceuticals Inc. 9e7568b6-52ae-4f7a-9bfd-503fd80a297e 2026-07-28 Warnings Exact identifier application number: M017 Aspercreme Lidocaine with Rosemary and Mint LIDOCAINE HYDROCHLORIDE Chattem, Inc. 9d40bfea-85d0-4943-83e9-0c16e79a011c 2026-07-28 Warnings Exact identifier application number: M017 KENS PAIN AND ARTHRITIS FORMULA MENTHOL Eezaway Relief Inc 35834473-3ad5-41ec-a110-e742aa7e2ee4 2026-07-28 Warnings Exact identifier application number: M017 DERMFREE Lidocaine 4% NUMBING Topical Anorectal Cream LIDOCAINE 4% NUMBING TOPICAL ANORECTAL CREAM Wenzhou Yuyuan Pharmaceutical Co., Ltd. 57935b64-6e2e-85d0-e063-6394a90a7428 2026-07-27 Warnings Exact identifier application number: M017 1% Hydrocortisone Anti-itch 1% HYDROCORTISONE ANTI-ITCH ALAINA HEALTHCARE PRIVATE LIMITED b8416467-55f7-4e5f-a5cb-3abd3e2bb577 2026-07-27 Warnings Exact identifier application number: M017 OWELL NATURALS ARTHRITIS MAXIMUM STRENGTH MENTHOL OWELL NATURAL 8 LLC 57984bc2-bf1d-c423-e063-6394a90a06ae 2026-07-27 Warnings Exact identifier application number: M017 Original Pain Relief TOPICAL ANALGESIC LOTION Real Time Pain Relief Inc 579bd303-9a50-4d66-e063-6294a90a6141 2026-07-27 Warnings Exact identifier application number: M017 Lidfix Pain Relief Patch Lidocaine LIDOCAINE HETERO HEALTHCARE LIMITED 2149f0e3-1983-4f02-929e-ecd20357f4bb 2026-07-27 Warnings Exact identifier application number: M017 RectoProtect LIDOCAINE Akron Pharma Inc. 1ca7d6cf-85a1-41a6-a07f-cff06a7edfbb 2026-07-27 Warnings Exact identifier application number: M017
Additional Listing Data#
Finished product Yes
Brand name base Jointflex
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 3.2 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2181415 Internal RxNorm lookup 2282659 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 72927-976-02 Jointflex 1 in 1 CARTON CREAM 1 4 72927-976-02 Jointflex 99 g in 1 TUBE, WITH APPLICATOR CREAM 99 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72927-976 JOINTFLEX (CAMPHOR) CREAM [STRIDES CONSUMER LLC] 4 Current NDC, Legacy NDC, 2 package rows 20250410_cb5ca02b-0bc1-4b0b-b4b1-abef3222aa56.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 72927-976-02 72927097602 1 TUBE, WITH APPLICATOR in 1 CARTON (72927-976-02) / 99 g in 1 TUBE, WITH APPLICATOR 2021-06-01 0000-00-00 No No Current