DRUG FACTS

Gold Edition Ultra Zheng Gu Shui by

Drug Labeling and Warnings

Gold Edition Ultra Zheng Gu Shui by is a Otc medication manufactured, distributed, or labeled by Guangxi Yulin Pharmaceutical Group Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GOLD EDITION ULTRA ZHENG GU SHUI- menthol camphor liquid 
Guangxi Yulin Pharmaceutical Group Co., Ltd.

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DRUG FACTS

Active ingredients

Menthol 4.09%.................................External analgesic

Camphor 4.09%.................……….…….External analgesic

Do not use otherwise than as directed

Keep out of reach of children

Keep out of reach of children to avoid accidental poisoning

If swallowed, get medical help or contact a Poison Control Center right away

If pregnant

If pregnant, ask a health professional before use

Directions

• Adults and children 12 years of age and older: Apply to the affected area not more than 3 to 4 times daily.
• Children under 12 years of age: Do not use or consult a doctor.

Other information

store at room temperature, 20 o to 25 oC(68 o to 77 oF)

Inactive ingredients

Aconitum kusnezoffii, Alocasia macrorrhiza,Angelica dahurica, Angelica pubescens,Ardisia crenata,Ardisia gigantifolia, Artocarpus styracifolius,Calophyllum membranaceum, Clematis chinensis, Cudrania cochinchinensis,Curcuma phaeocaulis,Cyathula officinalis,Cynanchum paniculatum, Ethanol,Eucommia ulmoides,Eupolyphaga sinensis,Kadsura coccinea,Millettia pulchra,Periploca sepium,Piper wallichii, Polygonum cuspidatum,Sarcandra glabra,Sparganium stoloniferum,Spatholobus suberectus

Questions?

+1-888-915-6789

M-F 9am to 5pm Pacific Time
You may report serious side effects to this phone number.

Purpose

External analgesic

Do not use

• on wounds
• irritated or damaged skin
• sensitive skin
• with a heating pad
• if pregnant
• with, or at the same time as, other external analgesic products
• if allergic to any ingredients of this product

When using this product

• avoid contact with the eyes or on mucous membranes
• do not bandage tightly
• do not apply to wounds or damaged skin
• do not use 1 hour before or after bathing

Stop use and ask a doctor if

• condition worsens
• symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days
• eexcessive irritation of the skin develops
• redness is present

Warnings

For external use only

Uses

For the temporary relief of minor aches and pains of muscles and joints due to:

• arthritis
• strains
• bruises
• sprains
• simple backache

GOLD EDITION ULTRA ZHENG GU SHUI 
menthol camphor liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59321-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	4.09 g  in 100 mL
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	4.09 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CYATHULA OFFICINALIS ROOT (UNII: BRM37UP34O)
SPARGANIUM STOLONIFERUM WHOLE (UNII: 873IV8AW3C)
CALOPHYLLUM MEMBRANACEUM ROOT (UNII: 6G661AA4F2)
ARTOCARPUS STYRACIFOLIUS ROOT (UNII: L1D54XX58F)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
CYNANCHUM PANICULATUM WHOLE (UNII: T14ONG8D7H)
ALCOHOL (UNII: 3K9958V90M)
KADSURA COCCINEA WHOLE (UNII: 81P4AE27JI)
MILLETTIA PULCHRA WHOLE (UNII: 861IW7ATEH)
PIPER WALLICHII LEAFY TWIG (UNII: IZT4A4E63F)
CLEMATIS CHINENSIS ROOT (UNII: 8Z18N528CU)
EUCOMMIA ULMOIDES BARK (UNII: L878N1L0AR)
EUPOLYPHAGA SINENSIS (UNII: 7USH1LF92M)
PERIPLOCA SEPIUM ROOT BARK (UNII: 638OW484M3)
POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
ANGELICA PUBESCENS ROOT (UNII: 0MF1EI01KJ)
ARDISIA GIGANTIFOLIA WHOLE (UNII: WEC9M7UOAG)
MACLURA COCHINCHINENSIS ROOT (UNII: 3WTU9E1VPU)
SARCANDRA GLABRA WHOLE (UNII: YI11034BNN)
ACONITUM KUSNEZOFFII ROOT (UNII: 3L29I4K8KX)
ALOCASIA MACRORRHIZOS WHOLE (UNII: P600HQ573H)
CURCUMA PHAEOCAULIS ROOT (UNII: P7PXC11S4S)
ARDISIA CRENATA ROOT (UNII: 74U2K67MND)
SPATHOLOBUS SUBERECTUS STEM (UNII: N51VZ363BA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59321-011-88	1 in 1 BOX	08/31/2022	12/31/2022
1		88 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/31/2022	12/31/2022

Labeler - Guangxi Yulin Pharmaceutical Group Co., Ltd. (653862581)

Registrant - Guangxi Yulin Pharmaceutical Group Co., Ltd. (653862581)

Establishment
Name	Address	ID/FEI	Business Operations
Guangxi Yulin Pharmaceutical Group Co., Ltd.		653862581	manufacture(59321-011)

Revised: 7/2025

Document Id: 3a78dcbc-7dfc-f8c6-e063-6394a90a02fc

34390-5

Set id: db126904-8858-4094-a2fe-8f23476f2610

Version: 2

Effective Time: 20250721

 

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