hydrating mouthspray

Manufacturer: Guangzhou Yanxi Biotechnology Co., Ltd
Effective date: 2024-11-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:35:27

Label at a glance#

Producthydrating mouthspray

Active ingredientMENTHOL, XYLITOL

Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Spray directly into mouth on the tongue.Rub tongue over teeth and gums for at least 5seconds.Use as needed.

WARNINGS SECTION

Keep out of children

INACTIVE INGREDIENT SECTION

Aqua

INDICATIONS & USAGE SECTION

For oral freshness

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of children

OTC - PURPOSE SECTION

Moistens and relieves symptoms of dry mouth

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84025-251

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
84025-251-01	2026-01-29	C162847	48780-1	49896155-a944-586f-e063-e6dba90add90	26615d91-0187-6c45-e063-6394a90acff0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84025-251-01	hydrating mouthspray	50 mL in 1 BOTTLE	LIQUID	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84025-251	HYDRATING MOUTHSPRAY LIQUID [GUANGZHOU YANXI BIOTECHNOLOGY CO., LTD]	1	1 package rows	20241109_26615d91-0187-6c45-e063-6394a90acff0.zip

Products#

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

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

hydrating mouthspray
MENTHOL
XYLITOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84025-251	84025-251-01

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
MENTHOL	L7T10EIP3A	ACTIB
XYLITOL	VCQ006KQ1E	ACTIB
WATER	059QF0KO0R	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
26615d91-0188-6c45-e063-6394a90acff0			26615d91-0187-6c45-e063-6394a90acff0	2024-11-08	Warnings	Exact identifier spl id: 26615d91-0188-6c45-e063-6394a90acff0 spl set id: 26615d91-0187-6c45-e063-6394a90acff0

Reported adverse events (FAERS/openFDA)#

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