FDA.reportPublic FDA data

Whitening Cream

Manufacturer
Yiwu Jingmo trade Co., LTD
Effective date
2024-11-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:37:40

Label at a glance#

ProductWhitening Cream
Active ingredientCOPPER TRIPEPTIDE-1
Label structure11 sections

Label contents#

Full prescribing information#

COMPONENTS

Copper Tripeptide-1：5%

OTC - PURPOSE SECTION

skin whitening

INDICATIONS & USAGE SECTION

Apply to skin until absorbed

WARNINGS SECTION

Prohibit ingestion by mouth.

Do not put into eyes or ears.

No contact with wounds

DOSAGE & ADMINISTRATION SECTION

For external use only.

OTC - DO NOT USE SECTION

Skin irritation occurs, wash with water, discontinue use

If symptoms do not improve, seek medical attention immediately

OTC - WHEN USING SECTION

Skin irritation occurs, wash with water, discontinue use

If symptoms do not improve, seek medical attention immediately。

Allow 5 minutes for the product to take effect

OTC - STOP USE SECTION

Wound breaks

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If sxralowed, get medical help or contact a Poison Conirol Cenler ngiht away

INACTIVE INGREDIENT SECTION

Aqua，Glycerin，Propylene Glycol，Palmitoyl Tripeptide-1，Palmitoyl Tetrapeptide-7，Palmitoyl Pentapeptide-4，，Pantothenic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84864-123-01Whitening Cream5 g in 1 BOXCREAM51
84864-123-02Whitening Cream15 g in 1 BOXCREAM151
84864-123-03Whitening Cream30 g in 1 BOXCREAM301
84864-123-04Whitening Cream50 g in 1 BOXCREAM501
84864-123-05Whitening Cream60 g in 1 BOXCREAM601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84864-123WHITENING CREAM CREAM [YIWU JINGMO TRADE CO., LTD]15 package rows20241118_2718510c-9404-5c36-e063-6394a90a9a58.zip

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
84864-12384864-123-01, 84864-123-02, 84864-123-03, 84864-123-04, 84864-123-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
COPPER TRIPEPTIDE-16BJQ43T1I9ACTIB
PALMITOYL TRIPEPTIDE-1RV743D216MIACT
PANTOTHENIC ACID19F5HK2737IACT
PALMITOYL TETRAPEPTIDE-7Q41S464P1RIACT
GLYCERINPDC6A3C0OXIACT
AQUA059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PALMITOYL PENTAPEPTIDE-4KK181SM5JGIACT

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
2718510c-9405-5c36-e063-6394a90a9a582718510c-9404-5c36-e063-6394a90a9a582024-11-17WarningsExact identifier
spl id: 2718510c-9405-5c36-e063-6394a90a9a58
spl set id: 2718510c-9404-5c36-e063-6394a90a9a58

Reported adverse events (FAERS/openFDA)#

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