dry mouth moisturizingspray

Manufacturer: Guangzhou Yanxi Biotechnology Co., Ltd
Effective date: 2024-11-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:38:39

Label at a glance#

Productdry mouth moisturizingspray

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 5 seconds.Use as needed.

WARNINGS SECTION

Keep out of children

INACTIVE INGREDIENT SECTION

Aqua

INDICATIONS & USAGE SECTION

For daily oral care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of children

OTC - PURPOSE SECTION

Rapidlyl, moistens and soothes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84025-267

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84025-267-01	dry mouth moisturizingspray	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
84025-267	DRY MOUTH MOISTURIZINGSPRAY LIQUID [GUANGZHOU YANXI BIOTECHNOLOGY CO., LTD]	1	1 package rows	20241123_277820ad-9991-361e-e063-6394a90af9e5.zip

Products#

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

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

dry mouth moisturizingspray
MENTHOL
XYLITOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84025-267	84025-267-01

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
277820ad-9992-361e-e063-6394a90af9e5			277820ad-9991-361e-e063-6394a90af9e5	2024-11-22	Warnings	Exact identifier spl id: 277820ad-9992-361e-e063-6394a90af9e5 spl set id: 277820ad-9991-361e-e063-6394a90af9e5

Reported adverse events (FAERS/openFDA)#

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