Home NDC 33217-001 CHING WAN HUNG SOOTHING HERBAL BALM
Product NDC 33217-001
11-digit product format 332170001
Labeler code 33217
Product ID 33217-001_3ab610b2-31c8-f996-e063-6394a90aa7c1
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form OINTMENT
Route TOPICAL
Labeler TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-10-25
Marketing end 2028-10-26
Substance MENTHOL
Active strength 1 g/100g
NDC exclude flag No
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 · 28 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 2025-04-01 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 33217-001-02 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 33217-001-01 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 33217-001-03 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 33217-001-02 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 33217-001-01 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 33217-001-03 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 33217-001-02 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 33217-001-01 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 33217-001-03 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 33217-001-02 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 33217-001-01 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 33217-001-03 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 33217-001-02 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 33217-001-01 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 33217-001-03 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 33217-001-02 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 33217-001-01 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 33217-001-03 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 33217-001-02 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 33217-001-01 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 33217-001-03 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 CHING WAN HUNG SOOTHING HERBAL BALM Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 1 g/100g
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 418610 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 33217-001-01 CHING WAN HUNG SOOTHING HERBAL BALM 10 g in 1 TUBE OINTMENT 10 4 33217-001-02 CHING WAN HUNG SOOTHING HERBAL BALM 30 g in 1 JAR OINTMENT 30 4 33217-001-03 CHING WAN HUNG SOOTHING HERBAL BALM 3 g in 1 TUBE OINTMENT 3 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded MENTHOL ACTIVE INGREDIENT L7T10EIP3A CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1 MENTHOL ACTIVE MOIETY L7T10EIP3A CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1 ANGELICA SINENSIS ROOT INACTIVE INGREDIENT B66F4574UG CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1 MYRRH INACTIVE INGREDIENT JC71GJ1F3L CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1 PISTACIA LENTISCUS RESIN INACTIVE INGREDIENT 7446H202QW CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1 QUINCE INACTIVE INGREDIENT 12MCS4H09N CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1 SAFFLOWER INACTIVE INGREDIENT 4VBL71TY4Y CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1 SANGUISORBA OFFICINALIS TOP INACTIVE INGREDIENT 09Q902660M CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1 SESAME OIL INACTIVE INGREDIENT QX10HYY4QV CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1 YELLOW WAX INACTIVE INGREDIENT 2ZA36H0S2V CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 33217-001 CHING WAN HUNG SOOTHING HERBAL BALM (MENTHOL) OINTMENT [TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.] 2 Current NDC, Legacy NDC, 3 package rows 20181016_ffadc904-8e9d-4cb8-815a-d583bbdb3f0b.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 126 of 151 · 3,010 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join equaline anti itch HYDROCORTISONE United Natural Foods, Inc. dba UNFI 83cd9f60-a4c4-4dea-97a7-cd96aade9e88 2024-09-24 Warnings Exact identifier application number: M017 good sense itch relief DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE L. Perrigo Company 162fe0a3-3995-4e6f-94ed-f839b2b0c80e 2024-09-24 Warnings Exact identifier application number: M017 Caring Mill Anti-Itch Cream DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE Veridian Healthcare 22ca137a-576c-a13c-e063-6394a90ae7fc 2024-09-23 Warnings Exact identifier application number: M017 Signature Care Anti Itch HYDROCORTISONE Safeway ed0eb068-3ce6-423d-a7f8-c3456b7f6040 2024-09-23 Warnings Exact identifier application number: M017 members mark hydrocortisone HYDROCORTISONE Sam's West Inc 218f0dcd-fa67-4935-8019-ecbbd53ed2f7 2024-09-23 Warnings Exact identifier application number: M017 anti itch HYDROCORTISONE Meijer, Inc. a07496e0-6fc2-4190-8a01-f513134ffb92 2024-09-23 Warnings Exact identifier application number: M017 ZYLOTROL PAIN RELIEVING LIDOCAINE HCL, MENTHOL Whitestone Products LLC 2301fed7-0fa9-450d-8b1b-006f53235be0 2024-09-21 Warnings Exact identifier application number: M017 Tibetree Cheezheng Joint Analgesic Patch CAMPHOR Tibet Cheezheng Tibetan Medicine Co. Ltd 65a8a63f-1864-473e-be72-7840a6a5dee7 2024-09-20 Warnings Exact identifier application number: M017 Cold Ice Analgesic Gel MENTHOL Dabur India Limited 22915b2f-5f76-3e38-e063-6394a90a07b4 2024-09-20 Warnings Exact identifier application number: M017 Exchange Select Hydrocortisone HYDROCORTISONE Army & Air Force Exchange Service 1b709db3-7dc1-4756-a8a0-dddda875dc57 2024-09-19 Warnings Exact identifier application number: M017 Lidocaine LIDOCAINE Stratus Pharmaceuticals Inc e1a8d4a7-01f7-4bab-8d09-875c461b3b61 2024-09-19 Warnings Exact identifier application number: M017 Camphor Spirit CAMPHOR 10% Strategic Sourcing Services, LLC 2216d799-7f6f-cab7-e063-6294a90a8d6c 2024-09-14 Warnings Exact identifier application number: M017 Meijer Analgesic Lidocaine Topical Analgesic LIDOCAINE HYDROCHLORIDE Meijer Distribution, Inc f5d39be6-3b91-4ba1-9015-fd3ffbbdf4aa 2024-09-12 Warnings Exact identifier application number: M017 leader anti itch DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE Cardinal Health 110, LLC. dba Leader e1aab35b-80d9-4515-afb7-8c662bc5d028 2024-09-11 Warnings Exact identifier application number: M017 LactiGo MENTHOL LactiGo, Inc. 849c3601-2bc8-0991-e053-2a91aa0a5e7f 2024-09-03 Warnings Exact identifier application number: M017 Hempvana Ultra Strength Pain Relief Gel Platinum - Arthritis MENTHOL 8% Telebrands Corp c22cf1a5-0d5d-5ea5-e053-2995a90a333b 2024-09-02 Warnings Exact identifier application number: M017 Itch and Rash Cream HYDROCORTISONE Wildman Business Group 1f95757d-a434-f02a-e063-6294a90a2d12 2024-09-01 Warnings Exact identifier application number: M017 Lidocaine Hydrochloride LIDOCAINE HYDROCHLORIDE Wildman Business Group 1fd1a4b3-b6fd-0d4c-e063-6394a90a3680 2024-09-01 Warnings Exact identifier application number: M017 BIOSAVIA External Analgesic Pain Relief CAPSAICIN BIOSAVIA USA, LLC 814aa66b-7719-4a29-a84e-18290367e9c7 2024-08-28 Warnings Exact identifier application number: M017 Careland Plantar Fasciitis Hydrogel Pain Patches LIDOCAINE, MENTHOL Planet (Anhui) Pharmaceutical Co., Ltd. 0e2f29c2-2e95-4be0-b7e9-f1761a1321a5 2024-08-21 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 33217-001-01 33217000101 10 g in 1 TUBE (33217-001-01) 10 g 2023-10-25 2028-10-26 No No Current 33217-001-02 33217000102 30 g in 1 JAR (33217-001-02) 30 g 2023-10-25 2028-10-26 No No Current 33217-001-03 33217000103 3 g in 1 TUBE (33217-001-03) 3 g 2023-10-25 2028-10-26 No No Current