FDA.reportPublic FDA data

TEETH WHITENINGESSENCE

Manufacturer
Dongguan Haiyi Technology Co.,Ltd.
Effective date
2024-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:22:16

Label at a glance#

ProductTEETH WHITENINGESSENCE
Active ingredient.ALPHA.-TOCOPHEROL, MENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Mentholum

Vitamin E

Inactive ingredient

INACTIVE INGREDIENT SECTION

Sorbitol

Purpose section

OTC - PURPOSE SECTION

1. Protect the gumsProvides protein and protects enamel.
2.Whitening teethTeeth are as bright as pearls.
3. Remove stains from teethSay goodbye to the black and yellow teeth.
4. Fresh breathEliminate bad breath and make you confident

waring

WARNINGS SECTION

keep out of the reach of children; Before use, take a little smeartest on the back of the ear, if there is no allergy discomfort, youcan use it on the face

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 breastfeeding 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

1. Apply a thin amount of gel to the gums with a toothbrush.

2. Do this once daily for at least 1 minute, preferably at bedtime.

3. After using, spit out the gel and should not eat, drink or rinse for 30minutes for best results. Do not swallow the gel.

4. Use daily for best results.

Dosage

DOSAGE & ADMINISTRATION SECTION

Once a day in the morning and evening

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84732-023-012025-07-29C16284748780-13b156c62-33cb-fb37-e063-e6dba90a4e07232b76ac-8c1e-7cb8-e063-6394a90a6c78

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84732-023-01TEETH WHITENINGESSENCE4 mL in 1 TUBELIQUID41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84732-023TEETH WHITENINGESSENCE LIQUID [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]11 package rows20240930_232b76ac-8c1e-7cb8-e063-6394a90a6c78.zip

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
84732-02384732-023-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROLH4N855PNZ1ACTIB
SORBITOL506T60A25RIACT
MENTHOLL7T10EIP3AACTIB

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
232b76ac-8c1f-7cb8-e063-6394a90a6c78232b76ac-8c1e-7cb8-e063-6394a90a6c782024-09-28WarningsExact identifier
spl id: 232b76ac-8c1f-7cb8-e063-6394a90a6c78
spl set id: 232b76ac-8c1e-7cb8-e063-6394a90a6c78

Reported adverse events (FAERS/openFDA)#

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