LARTT MOUTHWASH- sodium fluoride liquid

Lartt mouthwash by

Drug Labeling and Warnings

Lartt mouthwash by is a Otc medication manufactured, distributed, or labeled by ECOWORLDPHARM CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

sodium fluoride

INACTIVE INGREDIENT

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

PURPOSE

Anticavity

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

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

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

DOSAGE & ADMINISTRATION

for dental use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LARTT MOUTHWASH 
sodium fluoride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61284-0014
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
XYLITOL (UNII: VCQ006KQ1E)
PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61284-0014-2	30 in 1 PACKAGE	10/05/2023
1	NDC: 61284-0014-1	13 mL in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	10/05/2023

Labeler - ECOWORLDPHARM CO.,LTD (688735061)

Registrant - ECOWORLDPHARM CO.,LTD (688735061)

Establishment
Name	Address	ID/FEI	Business Operations
ECOWORLDPHARM CO.,LTD		688735061	manufacture(61284-0014)