Home NDC 59321-056 ULTRA STRENGTH ZHENG GU SHUI
Product NDC 59321-056
11-digit product format 593210056
Labeler code 59321
Product ID 59321-056_39ee8407-942b-cb0f-e063-6394a90a20ad
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL AND CAMPHOR
Dosage form LINIMENT
Route PERCUTANEOUS
Labeler GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-04-04
Marketing end 2028-05-01
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 4.1; 4.1 g/100mL; g/100mL
NDC exclude flag No
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 ULTRA STRENGTH ZHENG GU SHUI Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 4.1 g/100mL MENTHOL 4.1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup L7T10EIP3A Internal UNII 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 59321-056-02 ULTRA STRENGTH ZHENG GU SHUI 88 mL in 1 BOTTLE, WITH APPLICATOR LINIMENT 88 3 59321-056-02 ULTRA STRENGTH ZHENG GU SHUI 1 in 1 BOX LINIMENT 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59321-056 ULTRA STRENGTH ZHENG GU SHUI (MENTHOL AND CAMPHOR) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD] 2 Current NDC, 2 package rows 20241127_53397663-044d-4e48-989b-2c6257af5f84.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 53 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join ZIMS MAX FREEZE LIDOCAINE HYDROCHLORIDE AND MENTHOL, KOBAYASHI Healthcare International, Inc. e364ff83-4aaf-4897-a7da-06581bc321f2 2025-12-18 Warnings Exact identifier application number: M017 Tiger Balm White Regular Strength CAMPHOR (SYNTHETIC) AND MENTHOL Haw Par Healthcare Ltd. f406161e-a9c4-47d1-8b21-93b1b7938063 2025-12-17 Warnings Exact identifier application number: M017 Resinol PETROLATUM AND RESORCINOL ResiCal, Inc. 03f57a4a-f94b-4ba6-b709-41cfb6e16261 2025-12-17 Warnings Exact identifier application number: M017 HealthWise Maximum Pain Relief LIDOCAINE Veridian Healthcare afc3c16d-0076-44b2-ae7e-5f36d4d8088e 2025-12-17 Warnings Exact identifier application number: M017 HealthWise Max Lidocaine plus Menthol LIDOCAINE, MENTHOL Veridian Healthcare f39a27da-6799-4fc6-97ca-101eac4a9360 2025-12-17 Warnings Exact identifier application number: M017 HealthWise Original Menthol MENTHOL Veridian Healthcare e4bfb6b0-545e-4fbc-8538-4f41a6be1025 2025-12-17 Warnings Exact identifier application number: M017 Welly Polka First Aid Kit HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE Dongguan Shenglian Tins Products Co., Ltd. d7c4314c-c4c6-4adf-b384-3ac7a7108319 2025-12-17 Warnings Exact identifier application number: M017 Frankincense and Myrrh Arthritis Pain Therapy MENTHOL Wise Consumer Products 2410a199-f4a3-da6c-e063-6394a90aaace 2025-12-17 Warnings Exact identifier application number: M017 Lidocaine LIDOCAINE, MENTHOL Vive Health LLC 462d3b24-643e-91da-e063-6394a90a0e1d 2025-12-17 Warnings Exact identifier application number: M017 Theragesic METHYL SALICYLATE Mission Pharmacal Company db6c0c77-0a20-d574-a98f-e6c9998b941f 2025-12-17 Warnings Exact identifier application number: M017 Teevodar Pain Relieving MENTHOL Sod-e Biotech Ltd 205b0fef-4f00-db2e-e063-6294a90a93b8 2025-12-17 Warnings Exact identifier application number: M017 Frankincense and Myrrh Arthritis Pain Relief MENTHOL WISE CONSUMER PRODUCTS CO. 116045df-891b-f370-e063-6294a90abe42 2025-12-17 Warnings Exact identifier application number: M017 Frankincense and Myrrh Intensive Foot Therapy MENTHOL Wise Consumer Products 23e56c6b-0f2b-721f-e063-6394a90a1ed0 2025-12-17 Warnings Exact identifier application number: M017 Tiger Balm Ultra Strength CAMPHOR (SYNTHETIC) AND MENTHOL Haw Par Healthcare Ltd. f0561804-e0f7-495d-9768-9b86a208c51e 2025-12-17 Warnings Exact identifier application number: M017 Kwan Loong METHYL SALICYLATE AND MENTHOL Haw Par Healthcare Ltd. 54bcb26e-786a-403e-9330-11ae9e3c013a 2025-12-17 Warnings Exact identifier application number: M017 Magsoothium Body Cooling Formula MENTHOL Ubu/Elements, Inc. f7fb6ac9-a920-a440-e053-6394a90aaa35 2025-12-16 Warnings Exact identifier application number: M017 Magsoothium CBD Body Lavender MENTHOL Ubu/Elements, Inc. f9b87fbe-b889-67a1-e053-6394a90acbcd 2025-12-16 Warnings Exact identifier application number: M017 Aquaphor Itch Relief HYDROCORTISONE Beiersdorf Inc b1d0333f-ba60-35d8-e053-2995a90af932 2025-12-16 Warnings Exact identifier application number: M017 Magsoothium CBD Body MENTHOL Ubu/Elements, Inc. 00b2ef34-42d7-523c-e063-6294a90a753d 2025-12-16 Warnings Exact identifier application number: M017 GENTLECARE HAND AND SKIN SANITIZER BENZALKONIUM CHLORIDE PARAGON SOLUTIONS US, INC. 16650277-fa62-485e-9a82-7763d2b50168 2025-12-16 Warnings Exact identifier application number: M017
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 59321-056-02 59321005602 1 BOTTLE, WITH APPLICATOR in 1 BOX (59321-056-02) / 88 mL in 1 BOTTLE, WITH APPLICATOR 2023-04-04 2028-05-01 No No Historical