REMBRANDT DEEPLY WHITE PLUS PEROXIDE- sodium monofluorophosphate paste, dentifrice

Rembrandt Deeply White Plus Peroxide by

Drug Labeling and Warnings

Rembrandt Deeply White Plus Peroxide by is a Otc medication manufactured, distributed, or labeled by Ranir LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Sodium Monofluorophosphate (0.884%)

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 amount used for brushing is accidentally swallowed, seek medical help or contact a Poison Control Center right away.

Directions

Adults and children 2 years of age and older: Brush teeth thoroughly (for at least 1 minute), preferable after each meal or at least twice a day, or as directed by a dentist or doctor. Children under 6 years of age: Use a pea-sized amount and instruct 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: Consult a dentist or doctor. Do not swallow.

Other information

Store at 20° - 25°C (68°-77°F).

Inactive ingredients

calcium pyrophosphate, water, glycerin, PEG-8, colloidal silicon dioxide, hydrogen peroxide, flavor, sodium lauryl sulfate, sodium saccharin, cellulose gum, xanthan gum, citric acid, sodium citrate, sucralose, trisodium ethylenediamine, PVP

Package/Label Principal Display Panel

D DEEPLY WHITE® + Peroxide

WHITER TEETH IN 3 DAYS

REMBRANDT®

ANTICAVITY FLUORIDE TOOTHPASTE WITH PEROXIDE

STRENGTHENS & RESTORES ENAMEL

Peppermint

NET WT 3.5 OZ (99.2 g)

INGREDIENTS AND APPEARANCE

REMBRANDT DEEPLY WHITE PLUS PEROXIDE 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66923-123
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.884 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CALCIUM PYROPHOSPHATE (UNII: X69NU20D19)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
XANTHAN GUM (UNII: TTV12P4NEE)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
SUCRALOSE (UNII: 96K6UQ3ZD4)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66923-123-23	1 in 1 CARTON	11/20/2023
1		99 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 Drug	M021	11/20/2023

Labeler - Ranir LLC (364567615)