LISTERINE ESSENTIAL CARE- sodium monofluorophosphate gel, dentifrice

Listerine Essential Care by

Drug Labeling and Warnings

Listerine Essential Care by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Sodium monofluorophosphate 0.76% (0.13% w/v fluoride ion)

Purpose

Anticavity

Use

aids in the prevention of dental cavities

Warnings

Keep out of reach of children under 6 years of age. If more than used for brushing is accidently swallowed, get medical help or contact a Poison Control Center right away.

Directions

• adults and children 2 years of age and older: brush teeth thoroughly, preferably after each meal or at least 2 times a day, or as directed by a dentist or physician.
  • children 2-6 years use a pea sized amount
  • instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing)
  • supervise children as necessary until capable of using without supervision.
• children under 2 years of age: ask a dentist or doctor

Other information

• Store at Room Temperature.

Inactive ingredients

Water, Sorbitol, Hydrated Silica, Glycerin, PEG-32, Sodium Lauryl Sulfate, Cellulose Gum, Sodium Saccharin, Eucalyptol, Methyl Salicylate, Thymol, Phosphoric Acid, Menthol, Sodium Phosphate, Xanthan Gum, Benzoic Acid, Flavor, Mentha Viridis (Spearmint) Leaf Oil, Disodium Phosphate, Blue 1, Yellow 10

Questions?

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

PRINCIPAL DISPLAY PANEL - 119 g Tube Carton

LISTERINE®
ESSENTIAL CARE®
FLUORIDE ANTICAVITY TOOTHPASTE
ORIGINAL GEL

POWERFUL MINT GEL

FRESHENS BREATH
THE LISTERINE® WAY

Kills the Germs
That Cause Bad Breath
Helps Prevent Cavities
Removes Stains

NET WT. 4.2 OZ. (119 g)

INGREDIENTS AND APPEARANCE

LISTERINE ESSENTIAL CARE 
sodium monofluorophosphate gel, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42002-411
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sodium Monofluorophosphate (UNII: C810JCZ56Q) (Fluoride Ion - UNII:Q80VPU408O)	Fluoride Ion	1.3 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sorbitol (UNII: 506T60A25R)
Hydrated Silica (UNII: Y6O7T4G8P9)
Glycerin (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
Sodium Lauryl Sulfate (UNII: 368GB5141J)
Carboxymethylcellulose Sodium, Unspecified Form (UNII: K679OBS311)
Saccharin Sodium (UNII: SB8ZUX40TY)
Eucalyptol (UNII: RV6J6604TK)
Methyl Salicylate (UNII: LAV5U5022Y)
Thymol (UNII: 3J50XA376E)
Phosphoric Acid (UNII: E4GA8884NN)
Menthol, Unspecified Form (UNII: L7T10EIP3A)
Sodium Phosphate (UNII: SE337SVY37)
Xanthan Gum (UNII: TTV12P4NEE)
Benzoic Acid (UNII: 8SKN0B0MIM)
Spearmint Oil (UNII: C3M81465G5)
Sodium Phosphate, Dibasic, Anhydrous (UNII: 22ADO53M6F)
Fd&C Blue No. 1 (UNII: H3R47K3TBD)
D&C Yellow No. 10 (UNII: 35SW5USQ3G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42002-411-09	1 in 1 CARTON	03/12/2012
1		119 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part355	03/12/2012

Labeler - Johnson & Johnson Consumer Inc. (002347102)