Lartt mouthwash

Manufacturer: ECOWORLDPHARM CO.,LTD
Effective date: 2024-04-05
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:10:42

Label at a glance#

ProductLartt mouthwash

Active ingredientSODIUM FLUORIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium fluoride

INACTIVE INGREDIENT SECTION

Glycerin, Xylitol, DL-Alanine, Stevia, Sea Salt, Green tea Extract., Chitosan, Ginger tincture, Licorice Extract, Panax Ginseng Root Extract, Centella Extract, Acetic acid, Sodium citrate, Citric Acid, Tea Tree Oil, Peppermint Oil, Eucalyptol, Shine Muscat Flavor Sorbic acid, Sodium carboxymethylcellulose, L-menthol, Purified water

OTC - PURPOSE SECTION

Anticavity

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Adult and over 12 years old

¡ Use twice a day after brushing your teeth with a toothpaste

¡ 30 seconds vigorously swish contents of one packet and spit out

¡ Do not swallow after rinsed

¡ Recommend do not eat or drink for 30 minutes after rinsed. It will be better results

¡ Supervise children as necessary until capable of suing withour supervision

¡ Consult with doctor or dentist before use if you have any injuries such as dental works in your mouth

WARNINGS SECTION

if more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

for dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
240698	sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse	PSN	2
240698	sodium fluoride 0.5 MG/ML Mouthwash	SCD	2
240698	sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61284-0014-2	2025-07-29	C162847	48780-1	3b156c62-3115-fb37-e063-e6dba90a4e07	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61284-0014-1	Lartt mouthwash	13 mL in 1 PACKAGE	LIQUID	13		2
61284-0014-2	Lartt mouthwash	30 in 1 PACKAGE	LIQUID	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61284-0014	LARTT MOUTHWASH (SODIUM FLUORIDE) LIQUID [ECOWORLDPHARM CO.,LTD]	2	2 package rows	20240406_1554b1b5-1ad8-a3f8-e063-6294a90a06e9.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Lartt mouthwash
sodium fluoride
FLUORIDE ION
XYLITOL
PANAX GINSENG ROOT OIL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
61284-0014	61284-0014-1, 61284-0014-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM FLUORIDE	8ZYQ1474W7	ACTIB
XYLITOL	VCQ006KQ1E	IACT
PANAX GINSENG ROOT OIL	P9T4K47OM0	IACT
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
155531b7-0071-e201-e063-6394a90a3178			1554b1b5-1ad8-a3f8-e063-6294a90a06e9	2024-04-05	Warnings	Exact identifier spl id: 155531b7-0071-e201-e063-6394a90a3178 spl set id: 1554b1b5-1ad8-a3f8-e063-6294a90a06e9

Reported adverse events (FAERS/openFDA)#

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