POVI DENTAL CARE

Manufacturer
DOCTOR PHARM
Effective date
2020-11-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:19

Label at a glance#

ProductPOVI DENTAL CARE
Active ingredientSODIUM FLUORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium Flouride

OTC - PURPOSE SECTION

Keeps it white and makes it strong.
Keep your mouth clean.
Refreshes the oral cavity.
Prevents tooth decay and removes bad breath.
Increases aesthetic effect.
Prevention of gingivitis, periodontitis (alveolar fistula)
Prevention of periodontal disease
Prevention of gum disease

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

Adults and children 6 years of age and older: Use twice a day after brushing your teeth with a toothpaste. Vigorously swish 10 milliliters of rinse between your teeth for 1 minute and then spit out. Do not swallow the rinse. Do not eat or drink for 30 minutes after rinsing. Instruct children under 12 years of age in good rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 6 years of age: consult a dentist or doctor.

WARNINGS SECTION

1.Maintain certain usage and capacity.
2.When using it for children, use it under the guidance and supervision of the guardian.
3.Do not swallow this product.
4.Use only for mouthwash. Do not use for any purpose other than use. If you swallow a large amount, consult your doctor immediately.
5.Children under 6 years of age should not be used without instructions from pharmacists or doctors.
5.Keep out of reach of children.
6.Avoid direct sunlight and keep it as cool as possible. 8) Do not insert any other containers for quality preservation.
7.Do not administer to the next patient.
1).Patients with iodine intolerance
2).Patients with thyroid dysfunction
3).Pregnant women or breastfeeding women who may be pregnant or pregnant

INACTIVE INGREDIENT SECTION

Water, glycerin, ethyl alcohol, xylitol, sodium bicarbonate, flavor, citric acid hydrate, enzymatically modified stevia, sodium benzoate, sodium chloride, caramel color, povidone iodide topical solution, l-menthol

DOSAGE & ADMINISTRATION SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label22label22

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313029sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral RinsePSN1
313029sodium fluoride 0.2 MG/ML MouthwashSCD1
313029sodium fluoride 0.02 % (fluoride ion 0.009 % ) Oral RinseSY1
313029sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral RinseSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81017-0001-12022-01-28C16284748780-1d6a99b39-cce4-a426-e053-dadaa90af4c2DOCTOR PHARM - POVI DENTAL CARE MOUTHWASH

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81017-0001-1POVI DENTAL CARE110 mL in 1 BOTTLEMOUTHWASH1101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81017-0001POVI DENTAL CARE (SODIUM FLUORIDE) MOUTHWASH [DOCTOR PHARM]1Legacy NDC, 1 package rows20201110_b3a30cef-251a-099e-e053-2995a90ad2a5.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81017-000181017-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
b3a3044d-a177-4731-e053-2995a90a99efb3a30cef-251a-099e-e053-2995a90ad2a52020-11-06WarningsExact identifier
spl id: b3a3044d-a177-4731-e053-2995a90a99ef
spl set id: b3a30cef-251a-099e-e053-2995a90ad2a5

Reported adverse events (FAERS/openFDA)#

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