Label: QUIP- sodium fluoride paste, dentifrice
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Contains inactivated NDC Code(s)
NDC Code(s): 69261-002-01, 69261-002-02 - Packager: Quip NYC Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 October 22, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions
- adults and children 2yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as instructed by a dentist
- do not swallow
- to minimize swallowing use a pea-sized amount in children under 6 years
- supervise children's brushing until good habits are established
- children under 2 years: ask a dentist
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
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SPL UNCLASSIFIED SECTION
quip
We design and deliver simple ways to keep your mouth healthy.
dentist guidance
We partner with experts to provide only the ingredients that truly keep teeth healthy.
designed to simplify
We designed a holistic oral care range to help simplify your routine at home or on the go.
delivered on time
We deliver fresh paste, brush heads and other essentials on schedule, shipped free!
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
QUIP
sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69261-002 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.23 g in 100 g Inactive Ingredients Ingredient Name Strength CARRAGEENAN (UNII: 5C69YCD2YJ) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) GLYCERIN (UNII: PDC6A3C0OX) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) SORBITOL (UNII: 506T60A25R) WATER (UNII: 059QF0KO0R) HYDRATED SILICA (UNII: Y6O7T4G8P9) SACCHARIN SODIUM (UNII: SB8ZUX40TY) XYLITOL (UNII: VCQ006KQ1E) HYDROGEN PEROXIDE (UNII: BBX060AN9V) MENTHOL (UNII: L7T10EIP3A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69261-002-01 1 in 1 CARTON 07/18/2018 1 133 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69261-002-02 1 in 1 CARTON 07/18/2018 2 24 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 07/18/2018 Labeler - Quip NYC Inc. (079453380)