FDA.reportPublic FDA data

YYNRHI NUMBING Creams

Manufacturer
Guangzhou ChuanMa International Trading Co.,Ltd.
Effective date
2025-07-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:08:43

Label at a glance#

ProductYYNRHI NUMBING Creams
Active ingredientMENTHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 1%......Topical Anesthetic

OTC - PURPOSE SECTION

Temporarily relieves minor pain anditching associated with minor skin irritations,

WARNINGS SECTION

Stop and ask a doctor
an allergic reaction occursIf symptoms such as redness, swelling, irritation, swelling, pain occur, or if the symptoms worsen.

INDICATIONS & USAGE SECTION

Do not use in large quantities.Do not exceed the recommended daily dosage unless directed by a doctorDo not use if you are allergic to the ingredients in this product or if the seal is broken or missing

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenIn case of accidental ingestion,seekmedical advice immediately or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Children under 2 years: Do not useFor children under the age of 12, please consult a doctorFor adults:Apply to affected area not more than 3 times daily. lf possible, clean the affected area with mildsoap and warm water, and make sure to rinse thoroughly.Avoid applying to large areas of thebody Use only as directed.

OTHER SAFETY INFORMATION

Other Information
Storage and HandlingStore between 15-30℃(59-86°F)Avoid freezing and excessive heatabove 40°C(104°F)

INACTIVE INGREDIENT SECTION

Aloe Vera Extract,Tocopherol (Vitamin E),Licorice Root Extract.Jojoba Seed Oil.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2475473menthol 1 % Topical CreamPSN1
2475473menthol 10 MG/ML Topical CreamSCD1
2475473menthol 1 % Topical CreamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85593-004-01YYNRHI NUMBING Creams60 g in 1 BOTTLECREAM601

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85593-00485593-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
JOJOBA OIL724GKU717MIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
MENTHOLL7T10EIP3AACTIB
LICORICE61ZBX54883IACT

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
55a42f4b-6711-17a3-e063-6394a90a94273afbb743-a5b3-ccb7-e063-6394a90a42412026-07-02WarningsExact identifier
spl set id: 3afbb743-a5b3-ccb7-e063-6394a90a4241

Reported adverse events (FAERS/openFDA)#

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