Label: POP FEELING PEACHY- sodium fluoride paste, dentifrice
- NDC Code(s): 53208-572-20
- Packager: LG H&H CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 17, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Use
- Warnings
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Directions
- adults and children 2 years of age and and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or 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 years: ask a dentist.
- Inactive Ingredients
- Questions?
- Principal Display Panel - 120 g Tube Carton
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INGREDIENTS AND APPEARANCE
POP FEELING PEACHY
sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53208-572 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.4 mg in 1 g Inactive Ingredients Ingredient Name Strength SORBITOL (UNII: 506T60A25R) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) NIACINAMIDE (UNII: 25X51I8RD4) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) WATER (UNII: 059QF0KO0R) ZINC STEARATE (UNII: H92E6QA4FV) GLYCERIN (UNII: PDC6A3C0OX) SODIUM PYROPHOSPHATE (UNII: O352864B8Z) POLOXAMER 407 (UNII: TUF2IVW3M2) SODIUM LAURYL SULFATE (UNII: 368GB5141J) XANTHAN GUM (UNII: TTV12P4NEE) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SUCRALOSE (UNII: 96K6UQ3ZD4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) XYLITOL (UNII: VCQ006KQ1E) HYDRATED SILICA (UNII: Y6O7T4G8P9) Product Characteristics Color Score Shape Size Flavor PEACH Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53208-572-20 1 in 1 CARTON 11/17/2023 1 120 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 11/17/2023 Labeler - LG H&H CO., LTD. (688276187) Establishment Name Address ID/FEI Business Operations Tai Guk Pharma. Co., Ltd. 689060246 manufacture(53208-572)