85248-172update

Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD
Effective date
2026-07-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-23 05:10:10

Label at a glance#

ProductPUVIDA NUMBING
Active ingredientMENTHOL
Label structure13 sections

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: Do not use, consult a doctor

Storage and handling

Store between 15-30℃(59-86F). Avoid freezing and excessive heat above 40 ℃(104°F).

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 5% (w/w)

Purpose

OTC - PURPOSE SECTION

External analgesic

Use

INDICATIONS & USAGE SECTION

For the temporary relief of pain and itching associated with minor burns, sunburn, insect bites and minor skin irritation

Warnings

WARNINGS SECTION

·For external use only
·If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor
·Do not use in large quantities, particularly over raw surfaces or blistered areas
·Avoid contact with eyes. If this happens, rinse thoroughly with water

Do not use

OTC - DO NOT USE SECTION

·Do not use in large quantities, particularly over raw surfaces or blistered areas

When Using

OTC - WHEN USING SECTION

·Avoid contact with eyes, lf this happens, rinse thoroughly with water.

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, irritation

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, irritation

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If pregnant or breast-feeding, ask a health professional before use

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older:
Apply to affected area not more than 3 to 4 times daily.
Children under 2 years of age: Do not use, consult a doctor

Other information

STORAGE AND HANDLING SECTION

Store between 15-30℃(59-86F). Avoid freezing and excessive heat above 40 ℃(104°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

55

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136979843981521GTIN-13: 6979843981521
EAN-13: 6979843981521
GTIN storage (14 digits): 06979843981521
db07d74be952fc2fe1c5620b46113bb7.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
85248-17285248-172-01

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-03-25full-release2026-06-01 01:51:42

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
PUVIDA NUMBINGMENTHOL 5% (W/W) NUMBINGJiangxi Yudexi Pharmaceutical Co., LTD4de4e317-2f4f-e5d6-e063-6394a90a06112026-07-20WarningsExact identifier
ndc (package): 85248-172-01
ndc (product): 85248-172
ndc11 (package): 85248017201
spl id: 5708eb40-9ebc-4146-e063-6394a90a0ed3
spl set id: 4de4e317-2f4f-e5d6-e063-6394a90a0611

Reported adverse events (FAERS/openFDA)#

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