CREST PLUS BAKING SODA AND PEROXIDE WHITENING WITH TARTAR PROTECTION- sodium fluoride paste, dentifrice

Crest Plus Baking Soda and Peroxide by

Drug Labeling and Warnings

Crest Plus Baking Soda and Peroxide by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Sodium fluoride 0.243% (0.16% w/v fluoride ion)

Purpose

Anticavity toothpaste

Use

helps protect against cavities

Warning

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

Directions

• adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist
  • do not swallow
  • to minimize swallowing use a pea-sized amount in children under 6
  • supervise children's brushing until good habits are established
• children under 2 yrs.: ask a dentist

Inactive ingredients

glycerin, hydrated silica, water, propylene glycol, sodium bicarbonate, tetrasodium pyrophosphate, sorbitol, PEG-12, flavor, sodium hydroxide, sodium lauryl sulfate, sodium saccharin, poloxamer 407, xanthan gum, cellulose gum, calcium peroxide, titanium dioxide

Questions?

1-800-492-7378

SPL UNCLASSIFIED SECTION

Dist. by Procter & Gamble, Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 119 g Tube Carton

New Formula with 2X Peroxide

Crest Plus

Baking Soda & Peroxide

Whitening

With Tartar Protection

Fresh Mint

Net Wt 4.2 OZ (119g)

INGREDIENTS AND APPEARANCE

CREST PLUS BAKING SODA AND PEROXIDE  WHITENING WITH TARTAR PROTECTION
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-814
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.6 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
HYDRATED SILICA (UNII: Y6O7T4G8P9)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
SORBITOL (UNII: 506T60A25R)
POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
POLOXAMER 407 (UNII: TUF2IVW3M2)
XANTHAN GUM (UNII: TTV12P4NEE)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
CALCIUM PEROXIDE (UNII: 7FRO2ENO91)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-814-24	1 in 1 CARTON	11/13/2023
1		68 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69423-814-42	1 in 1 CARTON	11/13/2023
2		119 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 69423-814-57	1 in 1 CARTON	11/13/2023
3		161 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 69423-814-82	1 in 1 CARTON	11/13/2023
4		232 g in 1 TUBE; Type 0: Not a Combination Product
5	NDC: 69423-814-11	2 in 1 CELLO PACK	11/13/2023
5		161 g in 1 TUBE; Type 0: Not a Combination Product
6	NDC: 69423-814-35	3 in 1 CARTON	11/13/2023
6		161 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	11/13/2023

Labeler - The Procter & Gamble Manufacturing Company (004238200)