Label: ANTISEPTIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 41250-072-12, 41250-072-69, 41250-072-77, 41250-072-86
- Packager: Meijer Distribution, Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 10, 2025
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- Official Label (Printer Friendly)
- TEP
- active ingredents
- Purpose
- Use
- Warnings
- Do not use
- Stop use and ask a dentist if
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredient
- Questions
- Disclaimer
- Adverse reaction
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principal display panel
NDC 41250-072-86
Compare to FreshBurst ®Listerine® Active Ingredients*
meijer®
Mouth
Rinse
Antigingivitis
Antiplaque
SPRING MINT ®
Kills germs that cause bad breath, plaque & the gum disease gingivitis
ADA Accepted
American Dental Association
- Helps prevent and reduce plaque
- Helps prevent and reduce gingivitis
33.8 FL OZ (1.05 QT) 1 L
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INGREDIENTS AND APPEARANCE
ANTISEPTIC
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-072 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK) EUCALYPTOL 0.92 mg in 1 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.42 mg in 1 mL METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 0.6 mg in 1 mL THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL 0.64 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) SORBITOL SOLUTION (UNII: 8KW3E207O2) 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-072-77 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/23/1996 04/04/2023 2 NDC:41250-072-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/23/1996 3 NDC:41250-072-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/23/1996 4 NDC:41250-072-69 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/23/1996 09/16/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 12/23/1996 Labeler - Meijer Distribution, Inc (006959555) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(41250-072)