Label: LUCKY SUPER SOFT WHITENING ANTI CAVITY- sodium monofluorophosphate paste, dentifrice
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Contains inactivated NDC Code(s)
NDC Code(s): 20276-553-01, 20276-553-04 - Packager: Delta Brands Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 28, 2018
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Keep out of the reach of children
- Warnings
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Directions
adults and children 2 yrs and older brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist or physician. children under 6 yrs to minimize swallowing use a pea-sized amount and brushing until good habits are established. children under 2 years: ask a dentist or physician
- Inactive ingredients
- Package Label
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INGREDIENTS AND APPEARANCE
LUCKY SUPER SOFT WHITENING ANTI CAVITY
sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:20276-553 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 7.6 mg in 1 g Inactive Ingredients Ingredient Name Strength POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CALCIUM CARBONATE (UNII: H0G9379FGK) ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) SODIUM SILICATE (UNII: IJF18F77L3) SODIUM LAURYL SULFATE (UNII: 368GB5141J) GLYCERIN (UNII: PDC6A3C0OX) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) HYDRATED SILICA (UNII: Y6O7T4G8P9) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL (UNII: 506T60A25R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color blue Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:20276-553-01 2 in 1 BOX 03/31/2017 1 NDC:20276-553-04 113 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 final part355 03/31/2017 Labeler - Delta Brands Inc (102672008)