mojito MINT dentistry

Manufacturer: Yangzhou Hongshengding Chemical Co.,Ltd.
Effective date: 2018-09-07
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:56:45

Label at a glance#

Productmojito MINT dentistry

Active ingredientSODIUM FLUORIDE

Label structure6 sections

Indications and uses

aids in the prevention of dental vavities.

Dosage and administration

Adults and children 2years of age and older:Brush teeth thoroughly,preferably after each meal or at least twice a day,or as directed by a dentist or doctor. Instruct Children under 6 years of age in good burshing and rinsing ahnbits(to mininize swallowing ).supervise children as necessary until catlble of using without supervision. Children under 2 years:Consult a dentist or doctor.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.24%

Purpose

OTC - PURPOSE SECTION

anticavity

Uses

INDICATIONS & USAGE SECTION

aids in the prevention of dental vavities.

Warnings

WARNINGS SECTION

Keep out of the reach of children under 6 years of age.if more than used for brushing is accidently swallowed,get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2years of age and older:Brush teeth thoroughly,preferably after each meal or at least twice a day,or as directed by a dentist or doctor.

Instruct Children under 6 years of age in good burshing and rinsing ahnbits(to mininize swallowing ).supervise children as necessary until catlble of using without supervision.

Children under 2 years:Consult a dentist or doctor.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

HYDRATED SILICA,HYDROXYETHYL CELLULOSE,WATER,CARBOXYMETHYLCELLULOSE,SACCHARIN SODIUM,SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS.SODIUM BENZOATE,SODIUM LAURYL SULFATE,SORBITOL,GLYCERIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

901

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
416783	sodium fluoride 0.24 % Toothpaste	PSN	2
416783	sodium fluoride 0.0024 MG/MG Toothpaste	SCD	2
416783	sodium fluoride 0.24 % (fluoride ion 0.13 % ) Toothpaste	SY	2
416783	sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste	SY	2
416783	sodium fluoride 0.24 % (fluoride ion 0.15 % ) Toothpaste	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71035-901-01	2020-01-31	C162847	48780-1	9d75b9cf-dff7-f424-e053-dadaa90a57ce	71035-901 mojito MINT dentistry
71035-901-02	2020-01-31	C162847	48780-1	9d75b9cf-dff7-f424-e053-dadaa90a57ce	71035-901 mojito MINT dentistry

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71035-901-01	mojito MINT dentistry	1 in 1 BOX	PASTE	1	2
71035-901-01	mojito MINT dentistry	72 in 1 CARTON	PASTE	72	2
71035-901-02	mojito MINT dentistry	1 in 1 BOX	PASTE	1	2
71035-901-02	mojito MINT dentistry	288 in 1 CARTON	PASTE	288	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71035-901	MOJITO MINT DENTISTRY (SODIUM FLUORIDE) PASTE [YANGZHOU HONGSHENGDING CHEMICAL CO.,LTD.]	2	Legacy NDC, 4 package rows	20180907_7269b13a-63f8-288a-e053-2a91aa0a7da4.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

mojito MINT dentistry
Sodium Fluoride
SORBITOL
HYDRATED SILICA
HYDROXYETHYL CELLULOSE (40 MPA.S AT 2%)
WATER
CARBOXYMETHYLCELLULOSE
GLYCERIN
FLUORIDE ION
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS
SODIUM BENZOATE
SODIUM LAURYL SULFATE
SACCHARIN SODIUM
SACCHARIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71035-901	71035-901-01, 71035-901-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SORBITOL	506T60A25R	IACT
HYDRATED SILICA	Y6O7T4G8P9	IACT
HYDROXYETHYL CELLULOSE (40 MPA.S AT 2%)	I2N4ZF9233	IACT
WATER	059QF0KO0R	IACT
CARBOXYMETHYLCELLULOSE	05JZI7B19X	IACT
GLYCERIN	PDC6A3C0OX	IACT
SODIUM FLUORIDE	8ZYQ1474W7	ACTIM
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS	SX01TZO3QZ	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
SACCHARIN SODIUM	SB8ZUX40TY	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
754464c1-a009-92c5-e053-2991aa0a0ae0			7269b13a-63f8-288a-e053-2a91aa0a7da4	2018-09-07	Warnings	Exact identifier spl id: 754464c1-a009-92c5-e053-2991aa0a0ae0 spl set id: 7269b13a-63f8-288a-e053-2a91aa0a7da4

Reported adverse events (FAERS/openFDA)#

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