ANTISPETIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash 
United Natural Foods, Inc. dba UNFI

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Equaline 072.003/072AL rev 2-072AN
Spring Mint Antiseptic Mouthrinse

Active ingredients

Eucalyptol 0.092%

Menthol 0.042%

Methyl salicylate 0.060%

Thymol 0.064%

Purpose

Antigingivitis, Antiplaque

Use

helps control plaque that leads to gingivitis

Warnings

for this product

Do not use

if you have painful or swollen gums, pus from the gum line, loose teeth or increased spacing between the teeth. See your dentist immediately. These may be signs of periodontitis, a serious form of gum disease.

Stop use and ask a dentist if

gingivitis, bleeding, or redness persists for more than 2 weeks.

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.

Directions

adults and children 12 years of age and older - vigorously swish 20 mL (2/3 FL OZ or 4 teaspoonfuls) between teeth for 30 seconds then spit out; do not swallow

children under 12 years of age - consult a dentist or doctor

Other information

cold weather may cloud this product. Its antiseptic properties are not affected. Store at room temperature (59⁰ - 77⁰F)

Inactive ingredients

water, alcohol 21.6%, sorbitol, poloxamer 407, benzoic acid, sodium saccharin, flavor,  sodium citrate, yellow no. 10,  green no.3

TEP

SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION.

Disclaimer

*This product is not manufatured or distriubted by Johnson & Johnson Corporation, owner of the registered trademark Listerine.

Adverse Reactions

Like it or let us make it right.

That's our quality promise.

855-423-2630

DISTRIBUTED BY UNFI

Providence, RI 02908 USA

DSP-TN-21091

DSP-MO-20087

Principal display panel

NDC 411163-072-12

compare to FreshBurst Listerine Antiseptic Mouthwash active ingredients*

EQUALINE

antispetic mouthrinse

antigingivitis/antiplaque

spring mint

1L (33.8 FL OZ)

image description

ANTISPETIC 
eucalyptol, menthol, methyl salicylate, thymol mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-072
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)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41163-072-121500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/28/2004
2NDC:41163-072-77500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/28/2004
3NDC:41163-072-131200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/28/200412/04/2016
4NDC:41163-072-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/28/2004
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)12/28/2004
Labeler - United Natural Foods, Inc. dba UNFI (943556183)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(41163-072)

Revised: 3/2024
Document Id: 132b7578-2644-8a24-e063-6294a90aee03
Set id: cce74940-ebf1-4fa4-9ef4-50619704d5cd
Version: 17
Effective Time: 20240308
 
United Natural Foods, Inc. dba UNFI