FDA.reportPublic FDA data

Kalaya Breath Refresh Antiseptic Oral Rinse-updated label for NDC

Manufacturer
WALMART INC. (see also Equate)
Effective date
2026-08-20
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
daily-update
Hydrated at
2026-08-22 01:01:03

Label at a glance#

ProductAntiseptic
Active ingredientEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
Label structure10 sections

Indications and uses

helps prevent and reduce plaque gingivitis

Dosage and administration

adults and children 12 years of age and older: vigorously swish 20 milliliters of rinse between your teeth twice a day for 30 seconds and then spit out. Do not swallow the rinse. children 6 years to under 12 years of age: supervise use children under 6 years of age: do not use

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Eucalyptol (0.092%)

Menthol (0.042%)

Methyl Salicylate (0.060%)

Thymol (0.064%)

Purposes

OTC - PURPOSE SECTION

Antiplaque/antigingivitis

Uses

INDICATIONS & USAGE SECTION

helps prevent and reduce

  • plaque
  • gingivitis

Warning

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

in children under 12 years of age.

Stop use and ask a dentist

OTC - STOP USE SECTION

  • gingivitis, bleeding, or redness persists for more than 2 weeks
  • you have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. These may be signs or symptoms of periodontitis, a serious form of gum disease.

Keep out of reach of children under 6 years of age

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and older: vigorously swish 20 milliliters of rinse between your teeth twice a day for 30 seconds and then spit out. Do not swallow the rinse.
  • children 6 years to under 12 years of age: supervise use
  • children under 6 years of age: do not use

Other information

OTHER SAFETY INFORMATION

  • store at room temperature
  • cold weather may cloud this product. Its antiseptic properties are not affected.
  • this rinse is not intended to replace brushing or flossing

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, alcohol (21.6% v/v), sorbitol, poloxamer 407, flavor, sodium benzoate, benzoic acid, sodium saccharin, FD&C green #3

Questions or comments

OTC - QUESTIONS SECTION

1-888-287-1915

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to Listerine® Cool Mint® active ingredient*

Antiseptic Mouthwash

Blue Mint

Kills germs that cause plague, gingivitis, bad breath

Helps to control and prevent plague that leads to gingivitis

Eucalyptol (0.092%)

Menthol (0.042%)

Methyl salicylate (0.060%)

Thymol (0.064%)

Antiplaque/antigingivitis

L (QT PT FL OZ)

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

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND OR UNDER CAP IS BROKEN OR MISSING.

DISTRIBUTED BY: Walmart Inc.,

Bentonville, AR 72716

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EQUATE Mouthwash Blue Mint
EQUATE Mouthwash Blue Mint

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130681131430418GTIN-13: 0681131430418
EAN-13: 0681131430418
GTIN-12: 681131430418
UPC-A: 681131430418
GTIN storage (14 digits): 00681131430418		mouthwash-blue-mint-1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79903-15179903-151-75, 79903-151-50, 79903-151-99

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
NameUNIIKind
EUCALYPTOLRV6J6604TKACTIB
MENTHOLL7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB
THYMOL3J50XA376EACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
SORBITOL506T60A25RIACT
POLOXAMER 407TUF2IVW3M2IACT
SODIUM BENZOATEOJ245FE5EUIACT
BENZOIC ACID8SKN0B0MIMIACT
SACCHARIN SODIUMSB8ZUX40TYIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72026-08-12daily-update2026-08-14 00:01:33
62025-07-11full-release2026-06-01 01:38:07
52024-08-22full-release2026-06-01 00:17:38

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AntisepticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLWALMART INC. (see also Equate)584b38ce-d1ef-4ecc-a887-7c96e7f9669f2026-08-20WarningsExact identifier
ndc (package): 79903-151-99
ndc (package): 79903-151-50
ndc (package): 79903-151-75
ndc (product): 79903-151
ndc11 (package): 79903015199
ndc11 (package): 79903015175
ndc11 (package): 79903015150
spl id: 9534f163-d0a8-4315-b99c-2fa3114d4e71
spl set id: 584b38ce-d1ef-4ecc-a887-7c96e7f9669f

Reported adverse events (FAERS/openFDA)#

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