FDA.reportPublic FDA data

DRUGGIST Brightening cream

Manufacturer
Shenzhen Xiaomai Manufacturing Co Ltd
Effective date
2024-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:00:10

Label at a glance#

ProductDRUGGIST Brightening cream
Active ingredientARBUTIN
Label structure12 sections

Dosage and administration

Use twice daily, in the morning and evening. Apply an appropriate amount of cream evenly tothe cleansed face and neck. Gently massage until fully absorbed. Increase frequency of use as needed based onskin condition.

Storage and handling

Store in a cool, dry place. "Avoid direct sunlight. Consult a dermatologist if you have any questions.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Arbutin

PURPOSE

OTC - PURPOSE SECTION

whiten skin

INDICATIONS

INDICATIONS & USAGE SECTION

whiten skin

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - STOP USE SECTION

Do not use on damaged or brokenskin.

When using this product

OTC - WHEN USING SECTION

Wnen using tnis product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions for use

DOSAGE & ADMINISTRATION SECTION

Use twice daily, in the morning and evening.
Apply an appropriate amount of cream evenly tothe cleansed face and neck.
Gently massage until fully absorbed.
Increase frequency of use as needed based onskin condition.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Arbutin
Aqua
Glycerin
Sodium Hyaluronate
Stearyl Alcohol
Propanediol
Hydrogenated Lecithin
Squalane
Retinol

Other Information

STORAGE AND HANDLING SECTION

Store in a cool, dry place. "Avoid direct sunlight.
Consult a dermatologist if you have any questions.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83872-193DRUGGIST BRIGHTENING CREAM CREAM [SHENZHEN XIAOMAI MANUFACTURING CO LTD]1Unmatched20240625_1ba186b0-71be-7e6a-e063-6294a90a1233.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83872-19383872-193-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
SQUALANEGW89575KF9IACT
GLYCERINPDC6A3C0OXIACT
ARBUTINC5INA23HXFACTIB
AQUA REGIAX3TT5X989EIACT
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER788QAG3W8AIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
1,3-PROPANEDIOL BIS(4-AMINOBENZOATE)8860R9ORQRIACT
22-HYDROGENATED RACEMIC CALCIPOTRIOL96516X6183IACT
3,5-DIBROMOSALICYLIC ACIDT5JO5UA21HIACT

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
3657651c-6b51-c64b-e063-6394a90aebe11ba186b0-71be-7e6a-e063-6294a90a12332025-05-30WarningsExact identifier
spl set id: 1ba186b0-71be-7e6a-e063-6294a90a1233

Reported adverse events (FAERS/openFDA)#

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