Home NDC 55621-004 TheraPlus
Product NDC 55621-004
11-digit product format 556210004
Labeler code 55621
Product ID 55621-004_08831525-5717-3c3d-e063-6394a90a5aed
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form OINTMENT
Route TOPICAL
Labeler Zhejiang Jingwei Pharmaceutical Co., Ltd.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-03-01
Substance MENTHOL; MENTHYL SALICYLATE, (+/-)-
Active strength 10; 15 g/100g; g/100g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 TheraPlus
Brand name suffix Plus
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 10 g/100g MENTHYL SALICYLATE, (+/-)- 15 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 43XOA705ZD Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 311499 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 55621-004-01 TheraPlus Plus 28 g in 1 TUBE OINTMENT 28 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded MENTHOL ACTIVE INGREDIENT L7T10EIP3A THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 MENTHYL SALICYLATE, (+/-)- ACTIVE INGREDIENT 43XOA705ZD THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 MENTHOL ACTIVE MOIETY L7T10EIP3A THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 SALICYLIC ACID ACTIVE MOIETY O414PZ4LPZ THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 LAURETH-23 INACTIVE INGREDIENT N72LMW566G THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 MINERAL OIL INACTIVE INGREDIENT T5L8T28FGP THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 STEARYL ALCOHOL INACTIVE INGREDIENT 2KR89I4H1Y THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 TROLAMINE INACTIVE INGREDIENT 9O3K93S3TK THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4 WATER INACTIVE INGREDIENT 059QF0KO0R THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55621-004 THERAPLUS PLUS (MENTHOL) OINTMENT [ZHEJIANG JINGWEI PHARMACEUTICAL CO., LTD.] 6 Current NDC, Legacy NDC, 1 package rows 20231025_d4119f84-eb60-4134-b58e-de13d9601199.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 33 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Hemp Magic Fast-Acting Pain Relief Cream MENTHOL Nexxus Capital LLC 4af69640-1413-868b-e063-6394a90a3989 2026-02-16 Warnings Exact identifier application number: M017 RelaxInk LIDOCAINE LIDOCAINE 4% Hambli Limited 49a1cf66-9bb1-b918-e063-6394a90a2ff6 2026-02-15 Warnings Exact identifier application number: M017 blue goo Pain Relieving MENTHOL 2.5% Garcoa, Inc. 7b9b5ac6-9568-464c-8096-0302a1e650df 2026-02-13 Warnings Exact identifier application number: M017 Methyl Salicylate 30 Percent Cream METHYL SALICYLATE Alexso, Inc 1d50ccb2-1a5d-49c7-8524-2f54eed63e85 2026-02-13 Warnings Exact identifier application number: M017 Antiseptic Mouth Rinse EUCALYPTOL, MENTHOL, METHYOL SALICYLATE, THYMOL Topco Associates LLC a38e91c1-7ac6-4a7f-a5a2-8d9166b1535a 2026-02-13 Warnings, Adverse reactions Exact identifier application number: M017 Gel Cooling Pain Relief MENTHOL Topco Associates LLC 80962394-a46f-48fd-8e0c-685dd1e500d7 2026-02-13 Warnings, Adverse reactions Exact identifier application number: M017 Banophen DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE Major Pharmaceuticals 9758d886-bd58-4eb2-a827-fa8e7fee2b7c 2026-02-13 Warnings Exact identifier application number: M017 Natureplex Hydrocortisone Hydro HYDROCORTISONE Natureplex, LLC 2fc6a148-34bb-4289-8588-32c1bb011b98 2026-02-13 Warnings Exact identifier application number: M017 Capsaicin 0.035 Percent CAPSAICIN Alexso, Inc 6d0bc1cc-e812-4753-b20c-c0357dd6deb5 2026-02-13 Warnings Exact identifier application number: M017 Swiftalyn Numbing Cream LIDOCAINE 4% GENUINE INNOVATION LTD 3f74c4a6-26f0-ddf7-e063-6394a90a1225 2026-02-12 Warnings Exact identifier application number: M017 PHARMBANNER Arnica Bruise Cream ARNICA BRUISE CREAM Shenzhen Xinxin Yunhai Technology Co., Ltd. 3c783061-8e2d-8a84-e063-6394a90a5265 2026-02-12 Warnings Exact identifier application number: M017 ETERNAL SPIRIT BEAUTY PAIN RELIEF WITH HEMP MENTHOL, CAMPHOR Worldwide Cosmetics, Inc 459d64a9-0538-57c8-e063-6394a90a6155 2026-02-12 Warnings Exact identifier application number: M017 Antiseptic Mouth Rinse EUCALYPTOL Walgreen Co. cba60e9d-5f12-4c56-9fa5-6ce1514fc2b0 2026-02-12 Warnings, Adverse reactions Exact identifier application number: M017 Medicated Body Powder MENTHOL Walmart Stores Inc afd337b7-d76e-f17a-e053-2a95a90abac7 2026-02-12 Warnings Exact identifier application number: M017 Lidocaine Hydrochloride 2% LIDOCAINE HYDROCHLORIDE Aldermed Inc. 4977b722-d08d-3d9e-e063-6294a90a9035 2026-02-12 Warnings Exact identifier application number: M017 Ice Gel ICE COLD ANALGESIC MENTHOL Jell Pharmaceuticals Pvt Ltd 4a8b3f84-8c45-eb94-e063-6394a90a3e73 2026-02-11 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Lidocaine Patch LIDOCAINE Walgreen Co. 41c4e9fe-e407-b22a-e063-6394a90a4b27 2026-02-10 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE CREAM 1% Aldermed Inc. 4a7f2c0e-5cf3-29cb-e063-6394a90a5d8d 2026-02-10 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET PAIN RELIEF 4a7f92d3-dd35-44a3-e063-6294a90ae004 2026-02-10 Warnings Exact identifier application number: M017 NICOVITO HEMORRHOID MASTER LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID MASTER Jiangxi Yudexi Pharmaceutical Co., LTD 4a5e24fa-959e-79b4-e063-6294a90a8f68 2026-02-09 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 55621-004-01 55621000401 28 g in 1 TUBE (55621-004-01) 28 g 2013-03-01 0000-00-00 No No Current