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NDC 11527-0704-42 Sodium Fluoride 5000 ppm Sensitive 57.5; 5.8 mg/mL; mg/mL Details

Sodium Fluoride 5000 ppm Sensitive 57.5; 5.8 mg/mL; mg/mL

Sodium Fluoride 5000 ppm Sensitive is a DENTAL GEL, DENTIFRICE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sheffield Pharmaceuticals LLC. The primary component is POTASSIUM NITRATE; SODIUM FLUORIDE.

Product Information

NDC	11527-0704
Product ID	11527-704_c850c90a-b9bc-44b7-b30c-3f297f3ae164
Associated GPIs	88409902774020
GCN Sequence Number	060841
GCN Sequence Number Description	sodium fluoride/potassium nit PASTE (ML) 1.1 %-5 % DENTAL
HIC3	D2A
HIC3 Description	FLUORIDE PREPARATIONS
GCN	27029
HICL Sequence Number	017889
HICL Sequence Number Description	SODIUM FLUORIDE/POTASSIUM NITRATE
Brand/Generic	Generic
Proprietary Name	Sodium Fluoride 5000 ppm Sensitive
Proprietary Name Suffix	n/a
Non-Proprietary Name	Sodium Fluoride1.1%, Potassium Nitrate 5%
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	GEL, DENTIFRICE
Route	DENTAL
Active Ingredient Strength	57.5; 5.8
Active Ingredient Units	mg/mL; mg/mL
Substance Name	POTASSIUM NITRATE; SODIUM FLUORIDE
Labeler Name	Sheffield Pharmaceuticals LLC
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED DRUG OTHER
Application Number	n/a
Listing Certified Through	2024-12-31

Package

Package Images

NDC 11527-0704-42 (11527070442)

Pricing Information
NDC Package Code	11527-704-42
Billing NDC	11527070442
Package	1 TUBE in 1 CARTON (11527-704-42) / 100 mL in 1 TUBE
Marketing Start Date	2020-03-26
NDC Exclude Flag	N
Price Per Unit	0.11328
Pricing Unit	ML
Effective Date	2024-02-21
NDC Description	SODIUM FLUORIDE SENSTV 5000PPM
Pharmacy Type Indicator	C/I
OTC	N
Explanation Code	1, 5
Classification for Rate Setting	G
As of Date	2024-02-21

This pricing file, entitled the NADAC (National Average Drug Acquisition Cost) files, provide state Medicaid agencies with covered outpatient drug prices by averaging survey invoice prices from retail community pharmacies across the United States. These pharmacies include independent retail community pharmacies and chain pharmacies. The prices are updated on a weekly and monthly basis

Standard Product Labeling (SPL)/Prescribing Information SPL 02f4cf0b-188c-4522-b759-ffe4a9d150e8 Details

SPL UNCLASSIFIED SECTION

SODIUM FLUORIDE 5000 ppm Sensitive toothpaste

Rx ONLY

DESCRIPTION:

Self-topical neutral fluoride toothpaste containing 1.1% (w/w) sodium fluoride and 5% potassium nitrate.

Active Ingredients:

Sodium Fluoride 1.1% (w/w)

Potassium Nitrate 5%

Inactive Ingredients:

Blue 1, Carrageenan, Cocamidopropyl Betaine, Flavor, Hydrated Silica, Mica, PEG-12, Poloxamer 407, Sodium Hydroxide, Sodium Laurryl Sulfate, Sodium Saccharin, Sorbitol, Titanium Dioxide, Water (purified), Yellow 10

CLINICAL PHARMACOLOGY:

Frequent topical applications to the teeth with preparations having a relatively high fluoride content increase tooth resistance to acid dissolution and enhance penetration of the fluoride ion into tooth enamel.

INDICATIONS AND USAGE:

A dental caries preventive and sensitive toothpaste; for twice daily self-applied topical use,following by rinsing, helps reduce the painful sensitivity of the teeth to cold, heat, acid, sweets or contact in adults patients and children 12 years of age and older. It is well established that 1.1% sodium fluoride is safe and extraordinarily effective as a caries preventive when applied frequently with mouthpiece applicators.1-4 Sodium Fluoride 5000 ppm Sensitive 1.1% sodium fluoride toothpaste with 5% potassium nitrate in a squeeze-tube is easily applied onto a toothbrush. This prescription toothpaste should be used twice daily in place of your regular toothpaste, unless otherwise instructed by your dental professional. May be used whether or not drinking water is fluoridated, since topical fluoride cannot produce fluorosis. (See WARNINGS for exception.)

CONTRAINDICATIONS:

Do not use in pediatric patients under age 12 years unless recommended by a dentist or physician.

WARNINGS:

Not for systemic treatment- Do not Swallow. Keep out of the reach of children. Children under 12 years of age, consult a dentist or physician. Note: Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. See your dentist if the problem persists or worsens. Do not use this product longer than 4 weeks unless recommended by a dentist or physician.

PRECAUTIONS:

General not for systemic treatment. DO NOT SWALLOW.

Carcinogenesis, Mutagenesis, Impairment of Fertility:

In a study conducted in rodents, no carcinogenesis was found in male and female mice and female rats treated with fluoride at dose levels ranging from 4.1 to 9.1 mg/kg of body weight. Equivocal evidence of carcinogenesis was reported in male rats treated with 2.5 and 4.1 mg/kg of body weight. In a second study, no carcinogenesis was observed in rats, males or females, treated with fluoride up to 11.3 mg/kg of body weight. Epidemiological data provide no credible evidence for an association between fluoride, either naturally occurring or added to drinking water, and risk of human cancer. Fluoride ion is not mutagenic in standard bacterial systems. It has been shown that fluoride ion has potential to induce chromosome aberrations in cultured human and rodent cells at doses much higher than those to which humans are exposed. In vivo data are conflicting. Some studies report chromosome damage in rodents, while other studies using similar protocols report negative results. Potential adverse reproductive effects of fluoride exposure in humans have not been adequately evaluated. Adverse effects on reproduction were reported for rats, mice, fox, and cattle exposed to 100 ppm or greater concentrations of fluoride in their diet or drinking water. Other studies conducted in rats demonstrated that lower concentrations of fluoride (5 mg/kg of body weight) did not result in impaired fertility and reproductive capabilities.

Pregnancy:

Teratogenic Effects Pregnancy Category B. It has been shown that fluoride crosses the placenta of rats, but only 0.01% of the amount administered is incorporated in fetal tissue. Animal studies (rats, mice, rabbits) have shown that fluoride is not a teratogen. Maternal exposure to 12.2 mg fluoride/kg of body weight (rats) or 13.1 mg/kg of body weight (rabbits) did not affect the litter size or fetal weight and did not increase the frequency of skeletal or visceral malformations. There are no adequate and well-controlled studies in pregnant women. However, epidemiological studies conducted in areas with high levels of naturally fluoridated water showed no increase in birth defects. Heavy exposure to fluoride during in utero development may result in skeletal fluorosis, which becomes evident in childhood.

Nursing Mothers:

It is not known if fluoride is excreted in human milk. However, many drugs are excreted in milk, and caution should be exercised when products containing fluoride are administered to a nursing woman. Reduced milk production was reported in farm-raised fox when the animals were fed a diet containing a high concentration of fluoride (98-137 mg/kg of body weight). No adverse effects on parturition, lactation, or offspring were seen in rats administered fluoride up to 5 mg/kg of body weight.

Pediatric Use:

Safety and effectiveness in pediatric patients below the age of 12 years have not been established. Please refer to the CONTRAINDICATIONS and WARNINGS sections.

ADVERSE REACTIONS:

Allergic reactions and other idiosyncrasies have been rarely reported. To report SUSPECTED ADVERSE REACTIONS, contact Sheffield Pharmaceuticals, LLC. at 1-800-222-1087 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

OVERDOSAGE:

Accidental ingestion of large amounts of fluoride may result in acute burning in the mouth and sore tongue. Nausea, vomitting, and diarrhea may occur soon after ingestion (within 30 minutes)and are accompanied by salivation, hematemesis, and epigastric cramping abdominal pain. These symptoms may persist for 24 hours. If less than 5 mg fluoride/kg body weight (i.e. less than 2.3 mg fluoride/lb body weight) have been ingested, give calcium (e.g.milk) orally to relieve gastrointestinal symptoms and observe for a few hours. If more than 5 mg fluoride/kg body weight (i.e. more than 2.3 mg fluoride/lb body weight) have been ingested, induce vomitting, give orally soluble calcium (e.g. milk, 5% calcium gluconate or calcium lactate solution) and immediately seek medical assistance. For accidental ingestion of more than 15 mg fluoride /kg of body weight (i.e. more than 6.9 mg fluoride/lb body weight), induce vomitting and admit immediately to a hospital facility. A treatment dose (a thin ribbon) of Sodium Fluoride 5000 ppm Sensitive contains approximately 2.5 mg fluoride. A 3.4 FLOZ (100 ml) tube contains approximately 575 mg fluoride.

DOSAGE AND ADMINISTRATION:

Follow these instructions unless otherwise instructed by your dental professional:

Adults and pediatric patients 12 years of age or older, apply at least a 1 inch strip of Sodium Fluoride 5000 ppm Sensitive onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute, expectorate, and rinse mouth thoroughly.
Use twice daily, (morning and evening) or as recommended by dentist or physician. Make sure to brush all sensitive areas of the teeth. Children under 12 years of age:consultant a dentist or physician.

SPL UNCLASSIFIED SECTION

	HOW SUPPLIED:	Mild Mint
	3.4 floz. (100ml) net wt. tube	NDC# 11527-704-42

STORAGE:

Store at Controlled Room Temperature, 20-25°C (68-77°F).

REFERENCES:

American Dental Association, Accepted Dental Therapeutics, Ed. 40, Chicago, ADA, 405-407(1984).
H.R. Englander et al., JADA, 75, 638-644 (1967).
H.R. Englander et al., JADA, 78, 783-787 (1969).
H.R. Englander et al., JADA, 82, 354-358 (1971).

PRINCIPAL DISPLAY PANEL - 100ml Tube

Wentworth NDC 11527-704-42

Sodium Fluoride 5000 ppm MILD MINT

Sensitive

1.1% Sodium Fluoride, 5% Potassium Nitrate

Prescription Strength toothpaste for Sensitive Teeth

3.4 FLOZ (100ml) Rx only

PRINCIPAL DISPLAY PANEL - 100 ml Carton

Wentworth NDC 11527-704-42

Sodium Fluoride 5000 ppm MILD MINT

Sensitive

1.1% Sodium Fluoride, 5% Potassium Nitrate

Prescription Strength toothpaste for Sensitive teeth

3.4 FLOZ (100ml) Rx only

INGREDIENTS AND APPEARANCE

SODIUM FLUORIDE 5000 PPM SENSITIVE

sodium fluoride1.1%, potassium nitrate 5% gel, dentifrice

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:11527-704
Route of Administration	DENTAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	5.8 mg in 1 mL
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844)	POTASSIUM NITRATE	57.5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
CARRAGEENAN (UNII: 5C69YCD2YJ)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
MICA (UNII: V8A1AW0880)
POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
POLOXAMER 407 (UNII: TUF2IVW3M2)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U)
SORBITOL (UNII: 506T60A25R)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
WATER (UNII: 059QF0KO0R)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Product Characteristics
Color	green	Score
Shape		Size
Flavor	PEPPERMINT	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:11527-704-42	1 in 1 CARTON	03/26/2020
1		100 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
UNAPPROVED DRUG OTHER		03/26/2020

Labeler - Sheffield Pharmaceuticals LLC (151177797)

Registrant - Sheffield Pharmaceuticals LLC (151177797)

Name	Address	ID/FEI	Business Operations
Establishment
Sheffield Pharmaceuticals LLC		151177797	MANUFACTURE(11527-704) , analysis(11527-704)

Revised: 4/2020

Document Id: c850c90a-b9bc-44b7-b30c-3f297f3ae164

Set id: 02f4cf0b-188c-4522-b759-ffe4a9d150e8

Version: 2

Effective Time: 20200401

Search by Drug Name or NDC

NDC 11527-0704-42 Sodium Fluoride 5000 ppm Sensitive 57.5; 5.8 mg/mL; mg/mL Details

Sodium Fluoride 5000 ppm Sensitive 57.5; 5.8 mg/mL; mg/mL

Product Information

Package

Package Images

NDC 11527-0704-42 (11527070442)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 02f4cf0b-188c-4522-b759-ffe4a9d150e8 Details

SPL UNCLASSIFIED SECTION

DESCRIPTION:

Active Ingredients:

Inactive Ingredients:

CLINICAL PHARMACOLOGY:

INDICATIONS AND USAGE:

CONTRAINDICATIONS:

WARNINGS:

PRECAUTIONS:

Carcinogenesis, Mutagenesis, Impairment of Fertility:

Pregnancy:

Nursing Mothers:

Pediatric Use:

ADVERSE REACTIONS:

OVERDOSAGE:

DOSAGE AND ADMINISTRATION:

SPL UNCLASSIFIED SECTION

STORAGE:

REFERENCES:

PRINCIPAL DISPLAY PANEL - 100ml Tube

PRINCIPAL DISPLAY PANEL - 100 ml Carton

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