ANTISEPTIC- eucalyptol, menthol, methyl salicylate, thymol liquid 
WALMART INC. (see also Equate)

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Kalaya Breath Refresh Antiseptic Oral Rinse-updated label for NDC

Active ingredient

Eucalyptol (0.092%)

Menthol (0.042%)

Methyl Salicylate (0.060%)

Thymol (0.064%)

Purposes

Antiplaque/antigingivitis

Uses

helps prevent and reduce

Warning

Do not use

in children under 12 years of age.

Stop use and ask a dentist

  • 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

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

Other information

Directions

Inactive ingredients

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

Questions or comments

1-888-287-1915

Principal display panel

Compare to Listerine® Cool Mint® active ingredient

Antiseptic Mouthwash

Eucalyptol (0.092%)

Menthol (0.042%)

Methyl salicylate (0.060%)

Thymol (0.064%)

Antiplaque/antigingivitis

Blue Mint

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

Eucalyptol (0.92%), Menthol (0.042%), Methyl Salicylate (0.060%), Thymol (0.064%)

EQUATE Antiseptic Mouthwash

ANTISEPTIC 
eucalyptol, menthol, methyl salicylate, thymol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-151
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK) EUCALYPTOL0.92 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.42 mg  in 1 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE0.6 mg  in 1 mL
THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL0.64 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
SORBITOL (UNII: 506T60A25R)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-151-751.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/30/2022
2NDC:79903-151-50500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/30/2022
3NDC:79903-151-992 in 1 PACKAGE12/30/2022
31.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35612/30/2022
Labeler - WALMART INC. (see also Equate) (051957769)

Revised: 1/2023
Document Id: 04fbe093-df3b-47a7-a7b3-23a70f43d411
Set id: 584b38ce-d1ef-4ecc-a887-7c96e7f9669f
Version: 3
Effective Time: 20230124
 
WALMART INC. (see also Equate)