Family Wellness

Manufacturer: Family Dollar Services Inc.
Effective date: 2021-08-23
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:42:02

Label at a glance#

ProductFamily Wellness Anticavity Fresh Mint

Active ingredientSODIUM FLUORIDE

Label structure10 sections

Storage and handling

Other information cold weather may cloud this product. Its antiseptic properties are not affected . Store at room temperature (59° - 77°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Sodium fluoride 0.0221%

OTC - PURPOSE SECTION

Purpose

Anticavity

INDICATIONS & USAGE SECTION

Useaids in the prevention of dental cavities

WARNINGS SECTION

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

adults and children 12 years of age and older: use twice daily after brushing your teeth with toothpaste; vigorously swish 10 mL (2 teaspoonfuls) between teeth for 1 minute then spit out; do not swallow
children under 12 years of age: consult a dentist or doctor

STORAGE AND HANDLING SECTION

Other information cold weather may cloud this product. Its antiseptic properties are not affected . Store at room temperature (59° - 77°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients water, sorbitol, alcohol 21.6%, flavors, poloxamer 407, sodium lauryl sulfate, phosphoric acid, sucralose and/or sodium saccharin, dibasic sodium phosphate, D&C red no. 33, FD&C blue no. 1, FD&C yellow no. 6.

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY: Midwood Brands, LLC

500 Volvo Parkway, Chesapeake, VA 23320

Made in Canada

* This product is not manufactured or distributed by Johnson & Johnson, distributor of Listerine®.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COMPARE TO LISTERINE® TOTAL CARE*

FAMILY wellness™

TOTAL HEALTH

FRESH MINT

MOUTHWASH

6 IN 1 FORMULA

Helps Prevent Cavities
Kills Germs that Cause Bad Breath
Helps Keep Mouth Feeling Clean
Freshens Breath
Helps Strengthen Enamel
Helps Strengthen Teeth

33.8 FL OZ (1000 mL)

Fresh Mint Mouthwash

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
313029	sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral Rinse	PSN	3
313029	sodium fluoride 0.2 MG/ML Mouthwash	SCD	3
313029	sodium fluoride 0.02 % (fluoride ion 0.009 % ) Oral Rinse	SY	3
313029	sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral Rinse	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55319-233-86	2023-01-30	C162847	48780-1	c7ccaba7-1d8e-fd44-e053-dadaa90aa01b	Family Wellness Fresh Mint Anticavity Mouthwash
55319-233-86	2021-08-23	C162847	48780-1	c7ccaba7-1d8e-fd44-e053-dadaa90aa01b	Family Wellness Fresh Mint Anticavity Mouthwash
55319-233-86	2021-07-23	C162847	48780-1	c7ccaba7-1d8e-fd44-e053-dadaa90aa01b	Family Wellness Fresh Mint Anticavity Mouthwash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55319-233-86	Family WellnessAnticavity Fresh Mint	1000 mL in 1 BOTTLE, PLASTIC	MOUTHWASH	1000		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55319-233	FAMILY WELLNESS ANTICAVITY FRESH MINT (SODIUM FLUORIDE) MOUTHWASH [FAMILY DOLLAR SERVICES INC.]	3	Legacy NDC, 1 package rows	20210824_8bd5f337-4308-77d4-e053-2a95a90aed79.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

Family Wellness Anticavity Fresh Mint
Sodium fluoride
D&C RED NO. 33
SORBITOL
PHOSPHORIC ACID
SUCRALOSE
POLOXAMER 407
SODIUM PHOSPHATE, DIBASIC
WATER
ALCOHOL
FD&C YELLOW NO. 6
FOOD YELLOW 3 FREE ACID
SODIUM LAURYL SULFATE
SACCHARIN SODIUM
SACCHARIN
FD&C BLUE NO. 1
FLUORIDE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55319-233	55319-233-86

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
D&C RED NO. 33	9DBA0SBB0L	IACT
SORBITOL	506T60A25R	IACT
PHOSPHORIC ACID	E4GA8884NN	IACT
SUCRALOSE	96K6UQ3ZD4	IACT
POLOXAMER 407	TUF2IVW3M2	IACT
SODIUM PHOSPHATE, DIBASIC	GR686LBA74	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT
FD&C YELLOW NO. 6	H77VEI93A8	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
SACCHARIN SODIUM	SB8ZUX40TY	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
SODIUM FLUORIDE	8ZYQ1474W7	ACTIB

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
ca3ea13f-05ce-4be9-e053-2a95a90ad42a			8bd5f337-4308-77d4-e053-2a95a90aed79	2021-08-23	Warnings	Exact identifier spl id: ca3ea13f-05ce-4be9-e053-2a95a90ad42a spl set id: 8bd5f337-4308-77d4-e053-2a95a90aed79

Reported adverse events (FAERS/openFDA)#

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