Quip Anticavity

Manufacturer
Quip NYC Inc.
Effective date
2025-01-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:54:09

Label at a glance#

ProductQuip Anticavity
Active ingredientSODIUM FLUORIDE
Label structure11 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Sodium fluoride 0.24% (0.14% w/v fluoride ion)

OTC - PURPOSE SECTION

Purpose

Anticavity

INDICATIONS & USAGE SECTION

Use

Aids in the prevention of dental cavities

WARNINGS SECTION

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Adults and children 2 years of age and older: brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.
  • Use only a pea-sized amount and instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing).
  • Supervise children as necessary until capable of using without supervision
  • Children under 2 years of age: consult a dentist or doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Glycerin, Water, Hydrated Silica, Sorbitol, Erythritol, Sodium Lauroyl Sarcosinate, Flavor, Xylitol, Cellulose Gum, Sucralose, Titanium Dioxide

SPL UNCLASSIFIED SECTION

Distributed by: quip NYC Inc., 45 Main Street, Brooklyn, NY 11201, USA

Questions? hello@getquip.com

Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

quip

Toothpaste

Anticavity Fluoride

Xylitol, vegan, SLS-free formula

Mint

180 USES PER TUBE

NET WT 4.7 OZ (133G)

Quip Mint 12-2020Quip Mint 12-2020

Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Anticavity Fluoride Toothpaste

Mint

quip

NET WT 4.7 OZ (133G)

2012 quip Mint2012 quip Mint

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
416783sodium fluoride 0.24 % ToothpastePSN5
416783sodium fluoride 0.0024 MG/MG ToothpasteSCD5
416783sodium fluoride 0.24 % (fluoride ion 0.13 % ) ToothpasteSY5
416783sodium fluoride 0.24 % (fluoride ion 0.14 % ) ToothpasteSY5
416783sodium fluoride 0.24 % (fluoride ion 0.15 % ) ToothpasteSY5

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69261-006-01Quip Anticavity1 in 1 CARTONPASTE, DENTIFRICE15
69261-006-01Quip Anticavity133 g in 1 TUBEPASTE, DENTIFRICE1335
69261-006-06Quip Anticavity133 g in 1 TUBEPASTE, DENTIFRICE1335
69261-006-07Quip Anticavity130 g in 1 TUBEPASTE, DENTIFRICE1305
69261-006-08Quip Anticavity130 g in 1 TUBEPASTE, DENTIFRICE1305
69261-006-08Quip Anticavity1 in 1 CARTONPASTE, DENTIFRICE15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69261-006QUIP ANTICAVITY (SODIUM FLUORIDE) PASTE, DENTIFRICE [QUIP NYC INC.]5Current NDC, Legacy NDC, 6 package rows20250201_b6d4cfe3-535e-9163-e053-2a95a90ae140.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69261-00669261-006-01, 69261-006-06, 69261-006-08, 69261-006-07

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Quip AnticavitySODIUM FLUORIDEQuip NYC Inc.b6d4cfe3-535e-9163-e053-2a95a90ae1402025-01-30WarningsExact identifier
ndc (package): 69261-006-01
ndc (package): 69261-006-08
ndc (package): 69261-006-07
ndc (package): 69261-006-06
ndc (product): 69261-006
ndc11 (package): 69261000606
ndc11 (package): 69261000607
ndc11 (package): 69261000601
ndc11 (package): 69261000608
spl id: 2cf1ff95-9c53-f4bd-e063-6294a90aed10
spl set id: b6d4cfe3-535e-9163-e053-2a95a90ae140

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.