Home NDC 55424-1398 Pain Relieving MUSFLEX
Product NDC 55424-1398
11-digit product format 554241398
Labeler code 55424
Product ID 55424-1398_191734b3-f360-4e02-9211-52c127c94788
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR (NATURAL), MENTHOL
Dosage form LOTION
Route TOPICAL
Labeler CHUNG KEE USA INTERNATIONAL INC
Application part348
Marketing category OTC MONOGRAPH FINAL
Marketing start 2013-01-09
Marketing end 0000-00-00
Substance CAMPHOR (NATURAL); MENTHOL
Active strength 56 mg/mL; mg/mL
NDC exclude flag E
Listing certified through 2018-12-31
Current FDA listing Historical FDA.report record 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 · 44 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 55424-1398-8 I Inactivated by FDA d630ba8d3edf…732f749b63fb…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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 55424-1398-8 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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 55424-1398-8 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55424-1398-8 Pain Relieving MUSFLEX 80 mL in 1 BOTTLE, SPRAY LOTION 80 2
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CAMPHOR (NATURAL) ACTIVE INGREDIENT N20HL7Q941 PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 MENTHOL ACTIVE INGREDIENT L7T10EIP3A PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 CAMPHOR (NATURAL) ACTIVE MOIETY N20HL7Q941 PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 MENTHOL ACTIVE MOIETY L7T10EIP3A PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 ALCOHOL INACTIVE INGREDIENT 3K9958V90M PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 ANGELICA BISERRATA ROOT INACTIVE INGREDIENT OJ90180B22 PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 CHINESE CINNAMON INACTIVE INGREDIENT WS4CQ062KM PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 EUCALYPTUS OIL INACTIVE INGREDIENT 2R04ONI662 PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 METHYL SALICYLATE INACTIVE INGREDIENT LAV5U5022Y PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 OCIMUM GRATISSIMUM LEAF OIL INACTIVE INGREDIENT AVG2506KDV PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 PANAX NOTOGINSENG ROOT INACTIVE INGREDIENT GQX1C1175U PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 POLYGONUM CUSPIDATUM ROOT INACTIVE INGREDIENT 7TRV45YZF7 PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 SAFFLOWER INACTIVE INGREDIENT 4VBL71TY4Y PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 WATER INACTIVE INGREDIENT 059QF0KO0R PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 ZEDOARY INACTIVE INGREDIENT 123C43G128 PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55424-1398 PAIN RELIEVING MUSFLEX (CAMPHOR (NATURAL), MENTHOL) LOTION [CHUNG KEE USA INTERNATIONAL INC] 2 Legacy NDC, 1 package rows 20130112_bc27a8df-49be-4d73-ba2c-2b10c1f7ad91.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 55424-1398-8 55424139808 80 mL in 1 BOTTLE, SPRAY 80 ml Historical