Label: GLISTER MULTI-ACTION FLUORIDE- sodium fluoride paste, dentifrice
- NDC Code(s): 10056-530-06, 10056-530-65
- Packager: Access Business Group, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 21, 2023
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warning
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Directions
- Do not swallow
- Adults and children 2 years and over: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist or doctor
- Instruct children under 6 years in good rinsing habits (to reduce swallowing)
- Supervise children as necessary until capable of using without supervision
- Children under 2 years, ask a dentist or doctor.
- Inactive Ingredients
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SPL UNCLASSIFIED SECTION
With regular brushing, glister multi-action fluoride toothpaste helps remove plaque. This product contains SYLODENT polishing agent which safely cleans and helps eliminate stains to whiten teeth. To enhance your overall oral health, use the complete glister oral care system
Trademark is used by Access under license.
- PRINCIPAL DISPLAY PANEL
- Package Labeling: 10056-530-06
- Package Labeling: 10056-530-65
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INGREDIENTS AND APPEARANCE
GLISTER MULTI-ACTION FLUORIDE
sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10056-530 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 2.1 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) HYDRATED SILICA (UNII: Y6O7T4G8P9) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM LAURYL SULFATE (UNII: 368GB5141J) XYLITOL (UNII: VCQ006KQ1E) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) XANTHAN GUM (UNII: TTV12P4NEE) SACCHARIN SODIUM (UNII: SB8ZUX40TY) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10056-530-65 1 in 1 BOX 04/11/2011 1 65 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:10056-530-06 1 in 1 BOX 04/11/2011 2 191 g in 1 TUBE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 04/11/2011 Labeler - Access Business Group, LLC (839830713)