OLELON NUMBING

Manufacturer
Guangzhou ChuanMa International Trading Co.,Ltd.
Effective date
2025-09-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:14:34

Label at a glance#

ProductOLELON NUMBING
Active ingredientMENTHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient :

1% Menthol .…
Purpose
Topical Analgesic

OTC - PURPOSE SECTION

UseFor the temporary relief of localized pain, itching ordiscomfort from minor skin irritations.

WARNINGS SECTION

Warnings For external use only. Avoid contact with the eyes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenIn case of accidental ingestion, seek medical helpimmediately.

INACTIVE INGREDIENT SECTION

Water, Propylene glycol, Carbomer Homopolymer, Glycerin,Edetate Disodium,Hydroxyacetophenone, 1,2-Hexanediol,Chrysanthellum Indicum Top, Purslane, Polyoxyl 40hydrogenated castor oil

INDICATIONS & USAGE SECTION

Directions Adults: Clean the affected area with mild soap and warmwater and rinse thoroughly, Gently dry by patting with toilettissue or a soft cloth before application of this product.Children under 12 years of age: consult a doctor.

DOSAGE & ADMINISTRATION SECTION

1.Clean hands and treatment area with mild soap andwarm water, rinse thoroughly, then gently pat dry.2.Apply a thick layer of numbing cream to the treatmentarea, making sure to cover both the treatment area andits surroundings.3.Wrap tightly with plastic wrap and wait 40 -60 minutes(Longer time, better effect.)4.Wipe away residue, and wait another 15 -25 minutes forthe numbness to peak.
5.Begin the procedure.

OTC - WHEN USING SECTION

When using this product Do not exceed the recommendeddaily dosage unless directed by a doctor. Certain personscan develop allergic reactions to the ingredients in this product.Do not put this product into the rectum by using finger.

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
85593-018-01OLELON NUMBING120 g in 1 BOTTLECREAM1201

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85593-01885593-018-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
55a3ff2d-d744-aca4-e063-6294a90a75973f72e766-3427-5bc4-e063-6394a90aa6732026-07-02WarningsExact identifier
spl set id: 3f72e766-3427-5bc4-e063-6394a90aa673

Reported adverse events (FAERS/openFDA)#

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