Whitening and anti-freckle cream

Manufacturer
Guangdong Miaolian Cosmetics Co., Ltd.
Effective date
2024-08-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:55:50

Label at a glance#

ProductWhitening and anti-freckle cream
Active ingredientXANTHAN GUM
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

1. Before use, perform a skin test on your arm and discontinue use if you have allergy symptoms or skin abnormalities.
2. For external use only, avoid contact with eyes when used
3. Keep out of reach of children

OTC - PURPOSE SECTION

For Face Whitening and Hydrating

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children.lf swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

water..

INDICATIONS & USAGE SECTION

to Whitening the skin, and nurture the skin barrier.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84507-02084507-020-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
XANTHAN GUMTTV12P4NEEACTIB
WATER059QF0KO0RIACT

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
211ef010-3918-47a6-e063-6394a90a10a820b90bd0-553e-67ca-e063-6394a90a032b2024-09-02WarningsExact identifier
spl set id: 20b90bd0-553e-67ca-e063-6394a90a032b

Reported adverse events (FAERS/openFDA)#

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