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 118 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ultra Strength Pain Relief Gel MENTHOL TELEBRANDS CORP d91b2e09-550e-4968-e053-2995a90ae323 2024-11-20 Warnings Exact identifier application number: M017 Hempvana Ultra Strength Pain Relief Cream LIDOCAINE 4% Telebrands Corp c3162ba8-ac2d-5a65-e053-2995a90af246 2024-11-20 Warnings Exact identifier application number: M017 Hempvana Ultra Strength Pain Relief LIDOCAINE TELEBRANDS CORP d91ba9b1-083f-32e9-e053-2a95a90a9bd1 2024-11-20 Warnings Exact identifier application number: M017 DynaRub PAIN RELIEVING CREAM Dynarex Corporation 7f853941-a2d7-ed26-e053-2991aa0aa9ee 2024-11-20 Warnings Exact identifier application number: M017 MYCO Clinic Pain Relief CAMPHOR, MENTHOL Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions bcdc0322-bc75-4662-9c5a-d1be1d055252 2024-11-20 Warnings Exact identifier application number: M017 MYCO Clinic Pain Relief MENTHOL Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions 604a30c9-2306-47a1-bd31-94b63639dd90 2024-11-20 Warnings Exact identifier application number: M017 MYCO Clinic Pain Relief CAMPHOR, MENTHOL Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions 0b489420-3b5c-43c5-aab4-0e3720acf9ce 2024-11-20 Warnings Exact identifier application number: M017 MYCO Clinic Pain Relief CAMPHOR, MENTHOL Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions dd906129-a787-4352-856d-d7a915031a6e 2024-11-20 Warnings Exact identifier application number: M017 Walgreens Arthritis Pain Relief Cream HISTAMINE DIHYDROCHLORIDE Walgreens Company 80d3031a-7fa9-4f5b-b85e-c7c6ef314801 2024-11-20 Warnings Exact identifier application number: M017 Anti-Itch Medicated Maximum Strength BENZOCAINE AND RESORCINOL Walgreens Company 7fd86dcb-edef-4d0d-b389-7ecea595fe67 2024-11-20 Warnings Exact identifier application number: M017 Walgreens Pain Relief BENZOCAINE Walgreens Company 7cee7234-32cd-4bf3-8a6c-0882585eec7f 2024-11-20 Warnings Exact identifier application number: M017 Walgreens Advanced Scar Gel ADVANCED SCAR GEL Walgreens Company 2c040475-a124-485c-933e-66b452f5ab46 2024-11-20 Warnings Exact identifier application number: M017 LidoPro Pain Relief CAPSAICIN AND LIDOCAINE Clinic Pharma 274611ea-7fc2-ba3f-e063-6294a90aa50f 2024-11-19 Warnings Exact identifier application number: M017 First Aid Only Sting Relief Pad BENZOCAINE Acme United Corporation 5087cbbd-1bbe-62ed-e054-00144ff8d46c 2024-11-19 Warnings Exact identifier application number: M017 Sting Relief Pad BENZOCAINE, ISOPROPYL ALCOHOL Acme United Corporation 6bb9a782-2394-4c8c-e053-2991aa0a08d4 2024-11-19 Warnings Exact identifier application number: M017 First Aid Only Sting Relief BENZOCAINE Acme United Corporation 697127d1-c02e-16d2-e053-2a91aa0a39fd 2024-11-19 Warnings Exact identifier application number: M017 First Aid Only Hydrocortisone 1% Anti-Itch HYDROCORTISONE Acme United Corporation e5597b11-b08e-99e1-e053-2a95a90a15a5 2024-11-19 Warnings Exact identifier application number: M017 Equate Cold Therapy Pain Relieving Roll-on Analgesic MENTHOL, UNSPECIFIED FORM Wal-Mart Stores, Inc. 4115f0ac-e12a-4e59-94f5-a47dcc7f8766 2024-11-18 Warnings Exact identifier application number: M017 Equate Cold Therapy Pain Relieving Analgesic MENTHOL, UNSPECIFIED FORM Wal-Mart Stores, Inc. ac6c2112-8692-4628-97d8-3a5a9f509766 2024-11-18 Warnings Exact identifier application number: M017 Equate Odor-Free Therapy Arthritis Analgesic TROLAMINE SALICYLATE Wal-Mart Stores, Inc. 1d73e7b6-c7f9-4680-b3e3-a954b91e1863 2024-11-18 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