QUIP- sodium monofluorophosphate paste, dentifrice

Quip by

Drug Labeling and Warnings

Quip by is a Otc medication manufactured, distributed, or labeled by Quip NYC Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Sodium monofluorophosphate 0.76% (0.1% w/v fluoride ion)

PURPOSE

Purpose

Anticavity toothpaste

INDICATIONS & USAGE

Use

aids in prevention of dental cavities

WARNINGS

Warnings

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Centre right away.

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

Inactive ingredients

calcium carbonate, sorbitol, water, sodium lauryl sulfate, hydrated silica, sodium carboxymethyl cellulose, flavor, sodium silicate, sodium benzoate, sodium saycharin

SPL UNCLASSIFIED SECTION

Distributor: quip NYC Inc.,

45 Main Street

Brooklyn, NY 11201, USA

Made in:India

Expiry: 3 years from the Manufacturing date shown on crimp of tube

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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

quip

mint anticavity toothpaste

3 MONTHS

NET WT 4.7oz (133g)

INGREDIENTS AND APPEARANCE

QUIP 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69261-001
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.76 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK)
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SODIUM SILICATE (UNII: IJF18F77L3)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69261-001-01	1 in 1 CARTON	10/01/2014	08/03/2020
1		133 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69261-001-02	1 in 1 CARTON	10/01/2014	08/03/2020
2		24 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 69261-001-03	1 in 1 CARTON	10/01/2014	08/03/2020
3		1 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	10/01/2014	08/03/2020

Labeler - Quip NYC Inc. (079453380)