FDA.reportPublic FDA data

PUVIDA SNOW BLEACH

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2025-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:40:40

Label at a glance#

ProductPUVIDA SNOW BLEACH
Active ingredientNIACINAMIDE
Label structure12 sections

Dosage and administration

1.Apply the product evenly onto clean skin. 2.Massage until fully absorbed. 3. Use daily for several weeks for best results.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

NIACINAMIDE 15%

Purpose

OTC - PURPOSE SECTION

elastic and smooth skin

Use

INDICATIONS & USAGE SECTION

Used to whiten or lighten skin pigmentation.

Warnings

WARNINGS SECTION

For external use only.

on damaged or broken skin.

on individwals aged 12 and under.

Do not use

OTC - DO NOT USE SECTION

Do not use Stop and ask a doctor.

IF irritation or allergic reactions develop.

When Using

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes confact with eyes.

Please test this cream on a small patch of your the inside of the arm if it is your first time using this cream.

Stop Use

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.WHEN USING THIS PRODUCT

Please clean your hands before use to ensure the best results from the product.

Ask Doctor

OTC - ASK DOCTOR SECTION

Discontinue use if signs of irritation or rash occur.WHEN USING THIS PRODUCT

Please clean your hands before use to ensure the best results from the product.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Apply the product evenly onto clean skin.

2.Massage until fully absorbed.

3. Use daily for several weeks for best results.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER , ASCORBIC ACID ，CENTELLA ASIATICA ，CHAMOMILE ，ALLANTOIN

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136974603693072GTIN-13: 6974603693072
EAN-13: 6974603693072
GTIN storage (14 digits): 06974603693072		Label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84010-05184010-051-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZIACT
CENTELLA ASIATICA7M867G6T1UIACT
NIACINAMIDE25X51I8RD4ACTIB
WATER059QF0KO0RIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
CHAMOMILEFGL3685T2XIACT

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
4a473131-d46c-4e2e-e063-6394a90ae34927e225d2-af7c-15a9-e063-6294a90aeb0c2026-02-07WarningsExact identifier
spl set id: 27e225d2-af7c-15a9-e063-6294a90aeb0c

Reported adverse events (FAERS/openFDA)#

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