Purple Teeth Powder

Manufacturer: Guangzhou Yanxi Biotechnology Co., Ltd
Effective date: 2024-11-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:38:16

Label at a glance#

ProductPurple Teeth Powder

Active ingredientALUMINUM HYDROXIDE, HYDRATED SILICA

Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

For Adults:brush teeth thoroughly,preferably after each meal or at least twice a day,or as directed by o dentist or physician

WARNINGS SECTION

Keep out of children

INACTIVE INGREDIENT SECTION

Aqua

INDICATIONS & USAGE SECTION

For daily teeth care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of children

OTC - PURPOSE SECTION

Deep cleaning teeth

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84025-266

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84025-266-01	Purple Teeth Powder	100 g in 1 BOTTLE	POWDER	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84025-266	PURPLE TEETH POWDER POWDER [GUANGZHOU YANXI BIOTECHNOLOGY CO., LTD]	1	1 package rows	20241122_27688e23-9b4f-54c1-e063-6394a90a823b.zip

Products#

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

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

Purple Teeth Powder
WATER
ALUMINUM HYDROXIDE
HYDRATED SILICA

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84025-266	84025-266-01

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALUMINUM HYDROXIDE	5QB0T2IUN0	ACTIB
HYDRATED SILICA	Y6O7T4G8P9	ACTIB

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
27688e23-9b50-54c1-e063-6394a90a823b			27688e23-9b4f-54c1-e063-6394a90a823b	2024-11-21	Warnings	Exact identifier spl id: 27688e23-9b50-54c1-e063-6394a90a823b spl set id: 27688e23-9b4f-54c1-e063-6394a90a823b

Reported adverse events (FAERS/openFDA)#

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