Label: CREST 3D WHITE ARCTIC FRESH- sodium fluoride paste, dentifrice

  • NDC Code(s): 37000-875-02, 37000-875-03, 37000-875-04, 37000-875-06, view more
    37000-875-07, 37000-875-08, 37000-875-10, 37000-875-15, 37000-875-27, 37000-875-30, 37000-875-33, 37000-875-38, 37000-875-41, 37000-875-42, 37000-875-50, 37000-875-54, 37000-875-56, 37000-875-77, 37000-875-99
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 13, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Sodium fluoride 0.243% (0.15% 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

    water, sorbitol, hydrated silica, disodium pyrophosphate, sodium lauryl sulfate, flavor, sodium hydroxide, cellulose gum, sodium saccharin, carbomer, polysorbate 80, mica, titanium dioxide, blue 1

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE,
    CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 76 g Tube Carton

    Crest


    3D WHITE

    FLUORIDE ANTICAVITY TOOTHPASTE

    NET WT 2.7 OZ (76 g)

    ENAMEL SAFE WHITENING

    ADVANCED
    Arctic Fresh

    removes 90% more surface stains*

    starts whitening after 1 brush

    artwork

  • INGREDIENTS AND APPEARANCE
    CREST 3D WHITE  ARCTIC FRESH
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-875
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    MICA (UNII: V8A1AW0880)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorPEPPERMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-875-031 in 1 CARTON01/18/201612/01/2021
    199 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:37000-875-041 in 1 CARTON01/18/201612/01/2021
    2136 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:37000-875-061 in 1 CARTON01/18/201612/01/2021
    3181 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:37000-875-071 in 1 CARTON06/01/201609/16/2019
    4198 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:37000-875-082 in 1 CARTON01/18/201612/01/2021
    599 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:37000-875-102 in 1 CARTON01/18/201612/01/2021
    6136 g in 1 TUBE; Type 0: Not a Combination Product
    7NDC:37000-875-42119 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/04/201812/01/2021
    8NDC:37000-875-153 in 1 CELLO PACK01/18/201612/01/2021
    81 in 1 CARTON
    8136 g in 1 TUBE; Type 0: Not a Combination Product
    9NDC:37000-875-993 in 1 CELLO PACK01/18/201607/13/2023
    91 in 1 CARTON
    9116 g in 1 TUBE; Type 0: Not a Combination Product
    10NDC:37000-875-772 in 1 CELLO PACK01/18/2016
    101 in 1 CARTON
    1076 g in 1 TUBE; Type 0: Not a Combination Product
    11NDC:37000-875-301 in 1 CARTON01/18/201607/13/2023
    1185 g in 1 TUBE; Type 0: Not a Combination Product
    12NDC:37000-875-411 in 1 CARTON01/18/201607/13/2023
    12116 g in 1 TUBE; Type 0: Not a Combination Product
    13NDC:37000-875-541 in 1 CARTON01/18/201607/13/2023
    13153 g in 1 TUBE; Type 0: Not a Combination Product
    14NDC:37000-875-271 in 1 CARTON09/01/2021
    1476 g in 1 TUBE; Type 0: Not a Combination Product
    15NDC:37000-875-501 in 1 CARTON09/01/2021
    15141 g in 1 TUBE; Type 0: Not a Combination Product
    16NDC:37000-875-381 in 1 CARTON09/01/2021
    16107 g in 1 TUBE; Type 0: Not a Combination Product
    17NDC:37000-875-022 in 1 CARTON09/01/2021
    17107 g in 1 TUBE; Type 0: Not a Combination Product
    18NDC:37000-875-333 in 1 CELLO PACK09/01/2021
    181 in 1 CARTON
    18107 g in 1 TUBE; Type 0: Not a Combination Product
    19NDC:37000-875-561 in 1 CARTON09/01/2021
    19158 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/18/2016
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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