Label: ANTISPETIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 55319-664-12, 55319-664-13, 55319-664-69, 55319-664-86
- Packager: Family Dollar Services, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 28, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
- Warnings
- Do not use
- Stop use and ask a dentist if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Disclaimer
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Adverse Reactions
DISTRIBUTED BY: MIDWOOD BRANDS, LLC
500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA
MADE IN THE US WITH US AND FOREIGN COMPONENTS.
100% SATISFACTION OR YOUR MONEY BACK
Not 100% satisfied? Return package and unused product within 30 days to the store of purchase for a refund (with receipt) or exchange.
DSP-TN-21091
DSP-MO-20087
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Principle Panel Display
Sealed with printed neckband for your protection.
Do not use if band around cap is broken or missing.
FAMILY WELLNESS ™
COMPARE TO COOL MINT ®LISTERINE ®ANTISEPTIC MOUTWASH*
BLUE MINT
ANTISEPTIC MOUTHRINSE
Antigingivitis/Antiplaque Mouthrinse
- Kills germs that cause bad breath, plaque and disease gingivitis gum disease
1.5 L (1.58 QT) 50.7 FL OZ
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INGREDIENTS AND APPEARANCE
ANTISPETIC
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55319-664 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 (UNII: 506T60A25R) POLOXAMER 407 (UNII: TUF2IVW3M2) BENZOIC ACID (UNII: 8SKN0B0MIM) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM BENZOATE (UNII: OJ245FE5EU) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55319-664-69 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/11/2011 2 NDC:55319-664-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/11/2011 3 NDC:55319-664-13 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/11/2011 01/14/2015 4 NDC:55319-664-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/07/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/11/2011 Labeler - Family Dollar Services, Inc (024472631) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(55319-664)