ANTISEPTIC MOUTH RINSE- eucalyptol, menthol, methyl salicylate, thymol mouthwash 
Consumer Product Partners, LLC

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Swan 072.003/072AN
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

Directions

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

Inactive ingredients

water, alcohol 21.6%, sorbitol, poloxamer 407, benzoic acid, sodium saccharin, flavor, sodium citrate, yellow 10, green 3

Disclaimer

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

Adverse reaction

DISTRIBUTED BY:

Vi-Jon

8515 Page Avenue

St. Louis, MO 63114

1-888-593-0593

Principal panel display

Sealed With Printed Neckband For Your Protection

swan ®

ANTISEPTIC

Mouth Rinse

spring mint ®

Kills Germs that Cause Bad Breath, Plaque & the Gum Disease Gingivits.

Compare to the active ingredients in FreshBurst ® Listerine ®*

ADA ACCEPTED

AMERICAN DENTAL ASSOCIATION

1 LITER (33.8 FL OZ)

image description

ANTISEPTIC MOUTH RINSE 
eucalyptol, menthol, methyl salicylate, thymol mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-072
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:11344-072-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/15/2009
2NDC:11344-072-69250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/15/2009
3NDC:11344-072-77500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/15/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)08/15/2009
Labeler - Consumer Product Partners, LLC (119091520)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(11344-072)

Revised: 3/2024
Document Id: 138d03bf-9967-6394-e063-6394a90ad4a8
Set id: b60be9d4-cf1c-4d4d-b15b-20630b0a4be4
Version: 2
Effective Time: 20240313
 
Consumer Product Partners, LLC