Label: HIMALAYA PINK SALT PURPLE COLOR CORRECTOR PLUS INTENSIVE WHITENING TOOTHPASTE- sodium fluoride paste, dentifrice
- NDC Code(s): 53208-592-10
- Packager: LG H&H Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 31, 2024
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- 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.
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Inactive ingredients
GLYCERIN, HYDRATED SILICA, SODIUM HEXAMETAPHOSPHATE, WATER, PEG-6, ZINC STEARATE, COCAMIDOPROPYL BETAINE, FLAVOR, SODIUM LAURYL SULFATE, CARRAGEENAN, POTASSIUM PHOSPHATE (tribasic), POTASSIUM PHOSPHATE (monobasic), POLOXAMER 407, SODIUM SACCHARIN, ALGIN, SODIUM CHLORIDE, TOCOPHERYL ACETATE, XANTHAN GUM, CI 42090, SUCRALOSE, TITANATED MICA, CI 17200
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- SPL UNCLASSIFIED SECTION
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SPL UNCLASSIFIED SECTION
- 2.9X tone-up effect in just one use by reducing yellowness**
- Clinically proven to white teeth 9.6X more than regular toothpaste*
- Formulated without parabens, gluten, phthalates, triclosan
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U.S. patented formula***
* Compared to regular toothpaste without SHMP.
** 38% higher prevention compared to regular toothpaste without SHMP.
*** Patent : US 11,701, 313 B2 - Principal Display Panel:
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INGREDIENTS AND APPEARANCE
HIMALAYA PINK SALT PURPLE COLOR CORRECTOR PLUS INTENSIVE WHITENING TOOTHPASTE
sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53208-592 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.5 mg in 1 g Inactive Ingredients Ingredient Name Strength POTASSIUM PHOSPHATE, TRIBASIC (UNII: 16D59922JU) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM) SODIUM ALGINATE (UNII: C269C4G2ZQ) SODIUM CHLORIDE (UNII: 451W47IQ8X) POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) ZINC STEARATE (UNII: H92E6QA4FV) HYDRATED SILICA (UNII: Y6O7T4G8P9) SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L) SODIUM LAURYL SULFATE (UNII: 368GB5141J) CARRAGEENAN (UNII: 5C69YCD2YJ) MICA (UNII: V8A1AW0880) D&C RED NO. 33 (UNII: 9DBA0SBB0L) POTASSIUM PHOSPHATE, MONOBASIC (UNII: 4J9FJ0HL51) XANTHAN GUM (UNII: TTV12P4NEE) SUCRALOSE (UNII: 96K6UQ3ZD4) POLOXAMER 407 (UNII: TUF2IVW3M2) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color purple Score Shape Size Flavor MINT (Vanilla) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53208-592-10 1 in 1 CARTON 05/31/2024 1 100 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 05/31/2024 Labeler - LG H&H Co.,Ltd. (688276187) Establishment Name Address ID/FEI Business Operations Tai Guk Pharma. Co., Ltd. 689060246 manufacture(53208-592)