FDA.reportPublic FDA data

QIAN LI ZHUI FENG PAIN RELIEVING

Manufacturer
MADISON ONE ACME INC | Zhejiang Dingtai Pharmaceutical Co., Ltd
Effective date
2025-11-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:43:01

Label at a glance#

ProductQIAN LI ZHUI FENG PAIN RELIEVING
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure15 sections

Storage and handling

Other information ■ keep container tightly closed 
■ store protected from light at 15 to 30 C (59 to 86 F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Camphor 10%
Menthol 15%
Methyl salicylate 48%

OTC - PURPOSE SECTION

Purpose
External analgesic
External analgesic
External analgesic

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings
For external use only

OTC - DO NOT USE SECTION

Do not use
■ on wounds
■ on irritated or damaged skin

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you have
■ any concerns about using this product

OTC - WHEN USING SECTION

When using this product
■ do not use otherwise than as directed

■ avoid contact with the eyes or mucous membranes

■ do not bandage tightly

■ do not apply heat to the area in the form of heating pads, hot water bottles, or lamps (doing so increases the risk of serious burns)

OTC - STOP USE SECTION

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

■ excessive irritation of the skin develops

■ nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs

■ you feel actual pain or experience blistering or burning after application (it is normal to feel a warming or cooling sensation)

■ when using for pain of arthritis:
   ■ pain persists for more than 10 days
   ■ redness is present
   ■ in conditions affecting children under 12 years of age

ADVERSE REACTIONS SECTION

Report any unexpected side effectsfrom the use of this product to the FDA MedWatch Program

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrento avoid accidental poisoning. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions
■ adults and children 3 years of age and older: apply several drops and rub Into the affected area not more than 3 to 4 times daily

■ children under 3 years of age: consult your physician

STORAGE AND HANDLING SECTION

Other information
■ keep container tightly closed

■ store protected from light at 15 to 30 C (59 to 86 F)

INACTIVE INGREDIENT SECTION

Inactive ingredients
angelica biserrata root, angelica sinensis root, chaenomeles lagenaria fruit, clematis chinensis root, corydalis yanhusuo tuber, gentiana macrophylla root, lavender oil, mineral oil, sinomenium acutum stem, and taxillus chinensis top.

OTC - QUESTIONS SECTION

Questions or comments?(888) 221-3496 M-F 9 am to 5 pm
■ you may also report serious side effects to this phone number

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

QIAN LI ZHUI FENG PAIN RELIEVING OIL

NDC 55614-690-01

EXTERNAL ANALGESIC

1.69 FL OZ (50 ML)
IMAGE OF BOXIMAGE OF BOX

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2462015camphor 10 % / menthol 15 % / methyl salicylate 48 % Topical OilPSN4
2462015camphor 100 MG/ML / menthol 150 MG/ML / methyl salicylate 480 MG/ML Topical OilSCD4
2462015camphor 10 % / menthol 15 % / methyl salicylate 48 % Topical OilSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55614-690-01QIAN LI ZHUI FENG PAIN RELIEVING1 in 1 BOXOIL14
55614-690-01QIAN LI ZHUI FENG PAIN RELIEVING50 mL in 1 BOTTLE, GLASSOIL504

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55614-69055614-690-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANGELICA BISERRATA ROOTOJ90180B22IACT
ANGELICA SINENSIS ROOTB66F4574UGIACT
CHAENOMELES LAGENARIA FRUITXBC17A15MUIACT
CLEMATIS CHINENSIS ROOT8Z18N528CUIACT
CORYDALIS YANHUSUO TUBER0TUP42692ZIACT
GENTIANA MACROPHYLLA ROOT6559FC0U1BIACT
LAVENDER OILZBP1YXW0H8IACT
MINERAL OILT5L8T28FGPIACT
SINOMENIUM ACUTUM STEMBBH96IEM66IACT
TAXILLUS CHINENSIS TOPQJ523LD71PIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
MENTHOLL7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32024-11-25full-release2026-06-01 00:39:00

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
QIAN LI ZHUI FENG PAIN RELIEVINGCAMPHOR, MENTHOL, AND METHYL SALICYLATEMADISON ONE ACME INC03a4fb7c-2328-409d-99c8-cbcf2b4a451f2025-11-10Warnings, Adverse reactionsExact identifier
ndc (package): 55614-690-01
ndc (product): 55614-690
ndc11 (package): 55614069001
spl id: 43470bed-f5dc-8f8f-e063-6294a90ae553
spl set id: 03a4fb7c-2328-409d-99c8-cbcf2b4a451f

Reported adverse events (FAERS/openFDA)#

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