WHITENING AND FRECKLE REMOVING ESSENCE

Manufacturer: Dongguan Haiyi Technology Co.,Ltd.
Effective date: 2024-10-31
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:32:29

Label at a glance#

ProductWHITENING AND FRECKLE REMOVING ESSENCE

Active ingredientHYALURONIC ACID

Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

HYALURONIC ACID

Inactive ingredient

INACTIVE INGREDIENT SECTION

VITAMIN C,VITAMIN B5, VITAMIN E, GLYCEROL,ARBUTIN.

Purpose section

OTC - PURPOSE SECTION

1.Whitening and removing spots

2. Brightening skin tone

3. Multiple antioxidant effects

4. Glossy and transparent skin

Warning

WARNINGS SECTION

1. Please use according to the instructions.

2. lf it accidentally gets into your eyes,please rinse with water immediately.

3. lfthere are any abnormalities on yourskin, please stop using it.

4. Please keep out of reach ofchildren.Prevent children from accidentallyswallowing, and pregnant womenshould use with caution.

stop use

OTC - STOP USE SECTION

This product may cause allergic reactions in asmall number of people.
lf youexperience any discomfort,please stop using it immediately.

not use

OTC - DO NOT USE SECTION

Not suitable for use by children, pregnantor breast feeding people.

OUT OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

INDICATIONS & USAGE SECTION

After cleansingand toning, take anappropriate amount ofessence andapply it on the face evenly, massagegently in circular motion until absorbed.Use it daily for better results.

Dosage

DOSAGE & ADMINISTRATION SECTION

take an appropriateamount,Use 2-3 times a week

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7	Product name	1	20171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
84732-078-01	2025-07-29	C162847	48780-1	3b156c62-2c47-fb37-e063-e6dba90a4e07	25c35cc8-23ee-bcad-e063-6394a90aeb5a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84732-078-01	WHITENING AND FRECKLE REMOVING ESSENCE	40 mL in 1 BOTTLE, PUMP	LIQUID	40		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84732-078	WHITENING AND FRECKLE REMOVING ESSENCE LIQUID [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]	1	1 package rows	20241102_25c35cc8-23ee-bcad-e063-6394a90aeb5a.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

WHITENING AND FRECKLE REMOVING ESSENCE
ARBUTIN
ASCORBIC ACID
.ALPHA.,.ALPHA.'-DIGLYCEROL
.ALPHA.-TOCOPHEROL
HYALURONIC ACID
PANTOTHENIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84732-078	84732-078-01

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
Name	UNII	Kind
ARBUTIN	C5INA23HXF	IACT
ASCORBIC ACID	PQ6CK8PD0R	IACT
.ALPHA.,.ALPHA.'-DIGLYCEROL	UC0A740LR3	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT
HYALURONIC ACID	S270N0TRQY	ACTIB
PANTOTHENIC ACID	19F5HK2737	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
25c35cc8-23ef-bcad-e063-6394a90aeb5a			25c35cc8-23ee-bcad-e063-6394a90aeb5a	2024-10-31	Warnings	Exact identifier spl id: 25c35cc8-23ef-bcad-e063-6394a90aeb5a spl set id: 25c35cc8-23ee-bcad-e063-6394a90aeb5a

Reported adverse events (FAERS/openFDA)#

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