ANIXIKE Numbing

Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD
Effective date
2026-03-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:50:46

Label at a glance#

ProductANIXIKE Numbing
Active ingredientMENTHOL
Label structure13 sections

Dosage and administration

■ Adults and children 12 years and older: Apply to affected area not more than 3 to 4 times daily. ■ Children under 12 years of age: Ask a doctor.

Storage and handling

■ Store between 15–30°C (59–86°F). Avoid freezing and excessive heat above 40°C (104°F).

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 5%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

■ Temporarily relieves local pain and discomfort of anorectal area

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

■ Do not apply to eyes, broken skin, or mucous membranes.
■ Do not put this product into the rectum by using fingers or any mechanical device or applicator.

When Using

OTC - WHEN USING SECTION

■ If swallowed, get medical help.
■ Do not use if allergic to any ingredients.
■ If pregnant or breastfeeding, ask a health professional before use.■ Do not apply to eyes, broken skin, or mucous membranes.
■ Do not put this product into the rectum by using fingers or any mechanical device or applicator.

Stop Use

OTC - STOP USE SECTION

■ Stop use and ask a doctor if condition worsens or symptoms persist.

■ Condition worsens or does not improve within 7 days.

■ Allergic reaction occurs to ingredients in this product.
■ Symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase.
■ Symptoms clear up and return within a few days.

Ask Doctor

OTC - ASK DOCTOR SECTION

■ Stop use and ask a doctor if condition worsens or symptoms persist.

■ Condition worsens or does not improve within 7 days.

■ Allergic reaction occurs to ingredients in this product.
■ Symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase.
■ Symptoms clear up and return within a few days.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ If swallowed, get medical help.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Adults and children 12 years and older: Apply to affected area not more than 3 to 4 times daily.
■ Children under 12 years of age: Ask a doctor.

Other information

STORAGE AND HANDLING SECTION

■ Store between 15–30°C (59–86°F). Avoid freezing and excessive heat above 40°C (104°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

■Water ,Carbomer 934,Propylene Glycol,Soybean Lecithin,.Alpha.-Tocopherol Acetate,Benzyl Alcohol.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

55

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039690menthol 5 % Topical CreamPSN1
1039690menthol 50 MG/ML Topical CreamSCD1
1039690menthol 5 % Topical CreamSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136979843981095GTIN-13: 6979843981095
EAN-13: 6979843981095
GTIN storage (14 digits): 06979843981095
60d9253cbde8a669738c8e9edc53af22.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85248-167-01ANIXIKE Numbing30 g in 1 BOTTLECREAM301
85248-167-02ANIXIKE Numbing50 g in 1 BOTTLECREAM501
85248-167-03ANIXIKE Numbing60 g in 1 BOTTLECREAM601
85248-167-04ANIXIKE Numbing80 g in 1 BOTTLECREAM801
85248-167-05ANIXIKE Numbing100 g in 1 BOTTLECREAM1001

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85248-16785248-167-01, 85248-167-02, 85248-167-03, 85248-167-04, 85248-167-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
ANIXIKE NumbingMENTHOL 5% NUMBINGJiangxi Yudexi Pharmaceutical Co., LTD4d5c52d7-8e81-b62f-e063-6394a90ad03e2026-03-19WarningsExact identifier
ndc (package): 85248-167-03
ndc (package): 85248-167-05
ndc (package): 85248-167-01
ndc (package): 85248-167-04
ndc (package): 85248-167-02
ndc (product): 85248-167
ndc11 (package): 85248016705
ndc11 (package): 85248016701
ndc11 (package): 85248016704
ndc11 (package): 85248016702
ndc11 (package): 85248016703
spl id: 4d5c52d7-8e82-b62f-e063-6394a90ad03e
spl set id: 4d5c52d7-8e81-b62f-e063-6394a90ad03e

Reported adverse events (FAERS/openFDA)#

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