Bclsks NUMBING

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:51:05

Label at a glance#

ProductBclsks NUMBING
Active ingredientMENTHOL
Label structure13 sections

Dosage and administration

·Cleanse targeted skin area, pat dry. ·Apply a thin layer to the affected area, not more than 3-4 times daily.

Storage and handling

Store at 15-30°C(59-86°F)·Protect from excessive heat and direct sunlight-· Use only as directed

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

menthol 1% (w/w)

Purpose

OTC - PURPOSE SECTION

External analgesic

Use

INDICATIONS & USAGE SECTION

·Temporarily relieves pain and itching due to: minor burns,sunburn, insect bites, scrapes, minor skin irritations

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

·on large areas of the body.·on broken, blistered, or abraded skin. · For those who are allergic to local anesthetics
such as menthol。

When Using

OTC - WHEN USING SECTION

·avoid contact with the eyes - ·do not bandage tightly or use with heating pad -· use only as directed

Stop Use

OTC - STOP USE SECTION

·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,iritation

Ask Doctor

OTC - ASK DOCTOR SECTION

·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,iritation

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

lf swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

·Cleanse targeted skin area, pat dry. ·Apply a thin layer to the affected area, not more than 3-4 times daily.

Other information

STORAGE AND HANDLING SECTION

Store at 15-30°C(59-86°F)·Protect from excessive heat and direct sunlight-· Use only as directed

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Carbomer934, propylene Glycol,Soybean Lecithin,.Alpha.-Tocopherol Acetate,Benzyl Alcohol.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136974603691665GTIN-13: 6974603691665
EAN-13: 6974603691665
GTIN storage (14 digits): 06974603691665
26aa8398e6bcf933571aafd86cebb347.jpg

DailyMed Product Concepts#

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

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
84010-24284010-242-01

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
4a45ea43-bfc1-502b-e063-6294a90afb22473bd2f2-bd00-2351-e063-6294a90aa3822026-02-07WarningsExact identifier
spl set id: 473bd2f2-bd00-2351-e063-6294a90aa382

Reported adverse events (FAERS/openFDA)#

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