FDA.reportPublic FDA data

dark spot lightening bar

Manufacturer
Shenzhen XiaoMai Manufacturing Co., Ltd.
Effective date
2024-05-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:02:38

Label at a glance#

Productdark spot lightening bar
Active ingredientTOCOPHEROL, HYALURONIC ACID, ASCORBIC ACID, KOJIC ACID, RETINOL
Label structure12 sections

Dosage and administration

Latherinto wet skin and rinse off immediately.Safe for body and face use.

Storage and handling

Please store in a cool,dry place away from direct sunlight.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Curcuma Longa (Turmeric) Root Powder: 5%
Hyaluronic Acid: 3%
Retinol: 3%
Collagen: 3%
Kojic Acid: 7%
Ascorbic Acid : 3%
Tocopherol : 3%

PURPOSE

OTC - PURPOSE SECTION

Moisturizing, whitening, reducing wrinkles and fine lines, reducing pigmentation, improving skin's luster and elasticity.

INDICATIONS

INDICATIONS & USAGE SECTION

Pigmentation

WARNINGS

WARNINGS SECTION

For external use only

Do not use

OTC - STOP USE SECTION

on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove

Stop use and ask a doctor

OTC - STOP USE SECTION

and ask a doctor if rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

.If swallowed,get medical help or contact Poison Control Center right away

Directions for use

DOSAGE & ADMINISTRATION SECTION

Latherinto wet skin and rinse off immediately.Safe for body and face use.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Stearic Acid: 15%
Lauric Acid: 9%
Glycerin: 18%
Sodium Hydroxide: 0.5%
Sodium Laureth Sulfate: 6%
Disodium EDTA: 0.7%
Sucrose Laurate: 2%
BHT: 0.6%
Propylene Glycol Dioleate: 3.1%
Decyl Glucoside: 7%
Shea Butter Oleyl Esters: 4%
PPG-25 Sorbitol: 2%
Olive Oil: 3%
PEG-10 Esters: 2%
HC Yellow No.5: 0.1%

Other Information

STORAGE AND HANDLING SECTION

Please store in a cool,dry place away from direct sunlight.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83872-142DARK SPOT LIGHTENING BAR (KOJIC ACID BAR SOAP DARK SPOT LIGHTENING BAR) SOAP [SHENZHEN XIAOMAI MANUFACTURING CO., LTD.]1Unmatched20240515_18512e3f-c513-3053-e063-6394a90af34c.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83872-14283872-142-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
TOCOPHEROLR0ZB2556P8ACTIB
DECYL GLUCOSIDEZ17H97EA6YIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
OLIVE OIL6UYK2W1W1EIACT
PROPYLENE GLYCOL DIOLEATE84T0LSN7U6IACT
HYALURONIC ACIDS270N0TRQYACTIB
ASCORBIC ACIDPQ6CK8PD0RACTIB
KOJIC ACID6K23F1TT52ACTIB
HC YELLOW NO. 5I844A312T7IACT
STEARIC ACID4ELV7Z65APIACT
LAURIC ACID1160N9NU9UIACT
GLYCERINPDC6A3C0OXIACT
RETINOLG2SH0XKK91ACTIB
SUCROSE LAURATE05Q7CD0E49IACT
SODIUM HYDROXIDE55X04QC32IIACT

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
3657e12d-8989-c52a-e063-6294a90a231118512e3f-c513-3053-e063-6394a90af34c2025-05-30WarningsExact identifier
spl set id: 18512e3f-c513-3053-e063-6394a90af34c

Reported adverse events (FAERS/openFDA)#

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