Gold Edition Ultra Zheng Gu Shui

Manufacturer
Guangxi Yulin Pharmaceutical Group Co., Ltd.
Effective date
2022-08-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:54:35

Label at a glance#

ProductGold Edition Ultra Zheng Gu Shui
Active ingredientCAMPHOR (NATURAL), MENTHOL
Label structure15 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints due to: arthritis strains bruises sprains simple backache

Dosage and administration

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.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

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

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

OTC - ASK DOCTOR SECTION

Do not use otherwise than as directed

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant, ask a health professional before use

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

+1-888-915-6789

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

Purpose

OTC - PURPOSE SECTION

External analgesic

Do not use

OTC - DO NOT USE SECTION

  • 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

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

  • 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

WARNINGS SECTION

For external use only

Uses

INDICATIONS & USAGE SECTION

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

  • arthritis
  • strains
  • bruises
  • sprains
  • simple backache

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter Package

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59321-011-882025-07-21C16284748780-11030e365-64d9-111a-e063-dadaa90a10e2Gold Edition Ultra Zheng Gu Shui
59321-011-882024-01-30C16284748780-11030e365-64d9-111a-e063-dadaa90a10e2Gold Edition Ultra Zheng Gu Shui

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59321-011GOLD EDITION ULTRA ZHENG GU SHUI (MENTHOL CAMPHOR) LIQUID [GUANGXI YULIN PHARMACEUTICAL GROUP CO., LTD.]1Legacy NDC20220903_db126904-8858-4094-a2fe-8f23476f2610.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59321-01159321-011-88

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3a78dcbc-7dfc-f8c6-e063-6394a90a02fcdb126904-8858-4094-a2fe-8f23476f26102025-07-21WarningsExact identifier
spl set id: db126904-8858-4094-a2fe-8f23476f2610

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.