LISTERINE NATURALS ANTICAVITY - HERBAL MINT- sodium fluoride mouthwash

Listerine Naturals Anticavity - Herbal Mint by

Drug Labeling and Warnings

Listerine Naturals Anticavity - Herbal Mint by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient

Sodium fluoride 0.02% (0.01% w/v fluoride ion)

Purpose

Anticavity

Use

aids in the prevention of dental cavities

Warnings

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:
  • use twice daily after brushing your teeth with a toothpaste
  • vigorously swish 10 ml (2 teaspoonfuls) of rinse between your teeth for 1 minute and then spit out
  • do not swallow the rinse
  • do not eat or drink for 30 minutes after rinsing
  • supervise children as necessary until capable of using without supervision
• Children under 12 years of age: consult a dentist or doctor

Other information

• store at room temperature
• cold weather may temporarily cloud this product

Inactive ingredients

water, sorbitol solution, alcohol (21.6%), poloxamer 407, flavor, eucalyptol, methyl salicylate, thymol, stevia rebaudiana leaf/stem extract, phosphoric acid, menthol, disodium phosphate

Questions?

call toll-free 888-222-0182 or 215-273-8755 (collect)

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Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 1.0 L Bottle Label

LISTERINE®
naturals™
FORMULA WITH FLUORIDE

ANTICAVITY MOUTHWASH

SODIUM FLUORIDE & ACIDULATED PHOSPHATE TOPICAL SOLUTION
Natural Fluoride Formula for
Stronger Teeth, Restores
Essential Minerals to Enamel
& Kills Bad Breath Germs

• *vs. LISTERINE® Fluoride rinses: HERBAL MINT

1.0L (1 Qt 1.8 Fl OZ)

IMPORTANT: READ
DIRECTIONS FOR PROPER USE.

INGREDIENTS AND APPEARANCE

LISTERINE NATURALS ANTICAVITY - HERBAL MINT 
sodium fluoride mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0322
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sodium Fluoride (UNII: 8ZYQ1474W7) (Fluoride ion - UNII:Q80VPU408O)	Fluoride ion	0.1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sorbitol (UNII: 506T60A25R)
Alcohol (UNII: 3K9958V90M)
Poloxamer 407 (UNII: TUF2IVW3M2)
Eucalyptol (UNII: RV6J6604TK)
Methyl Salicylate (UNII: LAV5U5022Y)
Thymol (UNII: 3J50XA376E)
Stevia Rebaudiuna Leaf (UNII: 6TC6NN0876)
Phosphoric Acid (UNII: E4GA8884NN)
Menthol, Unspecified Form (UNII: L7T10EIP3A)
Sodium Phosphate, Dibasic, Anhydrous (UNII: 22ADO53M6F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0322-1	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part355	12/20/2013

Labeler - Johnson & Johnson Consumer Inc. (002347102)