ZHENG GU SHUI

Product NDC: 59321-055
11-digit product format: 593210055
Labeler code: 59321
Product ID: 59321-055_436cb650-b183-07c4-e063-6294a90ae29d
Type: HUMAN OTC DRUG
Nonproprietary name: CAMPHOR, MENTHOL
Dosage form: LINIMENT
Route: PERCUTANEOUS; TRANSDERMAL
Labeler: GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-06-01
Marketing end: 2030-06-01
Substance: CAMPHOR (SYNTHETIC); MENTHOL
Active strength: 5.6; 5.6 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: ZHENG GU SHUI

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	5.6 g/100mL
MENTHOL	5.6 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 RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1366315	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
17552943-4f11-42d6-ad41-fbc53f2bbd9a	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
59321-055-01	ZHENG GU SHUI	100 mL in 1 BOTTLE	LINIMENT	100	5
59321-055-02	ZHENG GU SHUI	88 mL in 1 BOTTLE, WITH APPLICATOR	LINIMENT	88	5
59321-055-03	ZHENG GU SHUI	60 mL in 1 BOTTLE, SPRAY	LINIMENT	60	5
59321-055-04	ZHENG GU SHUI	30 mL in 1 BOTTLE	LINIMENT	30	5
59321-055-05	ZHENG GU SHUI	12 mL in 1 BOTTLE	LINIMENT	12	5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
CYNANCHUM PANICULATUM ROOT	INACTIVE INGREDIENT	CZP7EPR012	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
POLYGONUM CUSPIDATUM WHOLE	INACTIVE INGREDIENT	1VDG5Y5HS6	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
ZANTHOXYLUM NITIDUM ROOT	INACTIVE INGREDIENT	L2CQZ81759	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1
ZEDOARY	INACTIVE INGREDIENT	123C43G128	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59321-055	ZHENG GU SHUI (CAMPHOR, MENTHOL) LINIMENT [GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD]	3	Current NDC, Legacy NDC, 5 package rows	20241127_17552943-4f11-42d6-ad41-fbc53f2bbd9a.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 141 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Rite Aid Anti-itch	HYDROCORTISONE	Rite Aid	0c540422-1579-9217-e063-6294a90ad06a	2023-12-12	Warnings	Exact identifier application number: M017
Anti-itch Paraben Free	HYDROCORTISONE	Weeks & Leo Co., Inc.	0c5419c5-0929-7ca6-e063-6294a90ac0a7	2023-12-12	Warnings	Exact identifier application number: M017
Rite Aid Hydrocortisone	HYDROCORTISONE 1%	Rite Aid	0c580f96-7fe9-19df-e063-6394a90a5a22	2023-12-12	Warnings	Exact identifier application number: M017
Anti itch	HYDROCORTISONE	Weeks & Leo Co., Inc.	0c58b750-d3a6-5ed1-e063-6294a90a4321	2023-12-12	Warnings	Exact identifier application number: M017
Greencaine Blast	LIDOCAINE	ALMA Laboratories, Inc.	031e0065-4c8a-43d8-bc69-3efa3c6c0ae3	2023-12-12	Warnings	Exact identifier application number: M017
Ageless Pain Relief	METHYL SALICYLATE, MENTHOL	Isagenix International, LLC	3c7e493b-923d-44b1-9076-46c7894308d4	2023-12-12	Warnings, Adverse reactions	Exact identifier application number: M017
CVS Extra Strength Itch Stopping	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	CVS	857af609-9dd7-a07a-e053-2991aa0ab6ba	2023-12-11	Warnings	Exact identifier application number: M017
Rite Aid Extra Strength Itch Stopping	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	Rite Aid	0c4170dd-e1fa-d549-e063-6394a90a5c23	2023-12-11	Warnings	Exact identifier application number: M017
Westlake Itch Relief	DIPHENHYDRAMINE HCL, ZINC ACETATE	Westlake HB Pharma LLC	0c416ba6-b01f-0609-e063-6294a90ae2a1	2023-12-11	Warnings	Exact identifier application number: M017
CVS Regular Strength Itch Stopping	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	CVS	87473ace-d834-e43f-e053-2a95a90a819c	2023-12-11	Warnings	Exact identifier application number: M017
Katinko External Analgesic Oil	CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE	Greenstone Pharmaceutical Inc.	5881fc35-3293-4f0b-801a-afcd6feb9496	2023-12-08	Warnings	Exact identifier application number: M017
Katinko Pain And Itch Relieving	CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE	Greenstone Pharmaceutical Inc.	fe907fa4-4a01-4974-b71f-9cd980b4eaa2	2023-12-08	Warnings, Adverse reactions	Exact identifier application number: M017
Cycle	MENTHOL	La Mend, Inc.	cfc0bcde-ef91-1e6c-e053-2a95a90ab79e	2023-12-07	Warnings	Exact identifier application number: M017
Hemorrhoidal Pain Relief Cream	GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM	WALGREENS	03bbe146-f185-bcfa-e063-6394a90a85bf	2023-12-04	Warnings	Exact identifier application number: M017
Quatriderm Anti-itch	HYDROCORTISONE	OPMX LLC	83e59e10-9878-e5c2-e053-2a91aa0af25e	2023-12-04	Warnings	Exact identifier application number: M017
TACT	DIPHENHYDRAMINE HYDROCHLORIDE, MENTHOL	Sato Pharmaceutical Inc., Ltd.	b6e2ee24-69de-4dfd-9081-b9537b7a7bad	2023-12-04	Warnings	Exact identifier application number: M017
Overnight Cold Therapy Pain Relief	MENTHOL, UNSPECIFIED FORM	Walgreen Co.	2cbd0966-4cf9-4271-bd53-6672b1ed2a99	2023-12-04	Warnings	Exact identifier application number: M017
Prolayed Lidocaine Male Genital Desensitizer	LIDOCAINE	ViaDerma Distribution, Inc.	9c5ad0d0-ca7a-4321-9334-f06f3f6be18f	2023-12-02	Warnings	Exact identifier application number: M017
Liberdol Topical Analgesic	METHYL SALICYLATE, MENTHOL, CAMPHOR (SYNTHETIC)	ViaDerma Distribution, Inc	ab52cd0e-34fa-41c7-9ce7-1183c2aff8d8	2023-12-01	Warnings	Exact identifier application number: M017
Prolayed	LIDOCAINE	MATRIX MIXOLOGY, INC	ae317876-adb1-6d13-e053-2995a90a74af	2023-12-01	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1366315	camphor 5.6 % / menthol 5.6 % Topical Lotion	PSN	17552943-4f11-42d6-ad41-fbc53f2bbd9a	5
1366315	camphor 56 MG/ML / menthol 56 MG/ML Topical Lotion	SCD	17552943-4f11-42d6-ad41-fbc53f2bbd9a	5
1366315	camphor 5.6 % / menthol 5.6 % Topical Lotion	SY	17552943-4f11-42d6-ad41-fbc53f2bbd9a	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59321-055-01	59321005501	100 mL in 1 BOTTLE (59321-055-01)	100 ml	2025-06-01	2030-06-01	No	No	Current
59321-055-02	59321005502	88 mL in 1 BOTTLE, WITH APPLICATOR (59321-055-02)	88 ml	2025-06-01	2030-06-01	No	No	Current
59321-055-03	59321005503	60 mL in 1 BOTTLE, SPRAY (59321-055-03)	60 ml	2025-06-01	2030-06-01	No	No	Current
59321-055-04	59321005504	30 mL in 1 BOTTLE (59321-055-04)	30 ml	2025-06-01	2030-06-01	No	No	Current
59321-055-05	59321005505	12 mL in 1 BOTTLE (59321-055-05)	12 ml	2025-06-01	2030-06-01	Yes	No	Current