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OTC products · Product label record

Dentalclean Advanced Pro drug information

SODIUM FLUORIDE 0.24%
Rabbit Indstria e Comrcio de Produtos de Higiene Pessoal Ltda · DENTAL

Product NDC: 84035-013

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Generic nameSODIUM FLUORIDE 0.24%
Labeler / manufacturerRabbit Indstria e Comrcio de Produtos de Higiene Pessoal Ltda
RouteDENTAL
Drug classDrug class not supplied in source label
Product NDC84035-013
Label effective date2026-09-04

Official product label reference

Dentalclean Advanced Pro — Rabbit Indstria e Comrcio de Produtos de Higiene Pessoal Ltda

This page contains 7 source sections for SODIUM FLUORIDE 0.24%, dental route. Label set 4d261dc8-b065-567f-e063-6294a90aa93f, version 3.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use • Aids in the prevention of cavities • Helps prevent gingivitis •Helps interfere with harmful effects of plaque associated with gingivitis • Builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact.

Purpose

Anticavity
Dosage and administration — label text
Directions Adults and children 12 years of age and older: apply at least a 1 inch strip of the product onto a soft bristled toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist. Make sure to brush all sensitive areas of the teeth. Do not swallow. Children under 12 year of age: consult a dentist.
Warnings
WARNINGS: When using this product for sensitivity , do not use longer than 4 weeks unless recommended by a dentist. Stop use and ask a dentist if the sensitivity problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. Keep out of children. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away. Stop use and ask a dentist if • gingivitis, bleeding, or redness persists for more than 2 weeks • you have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. These may be signs of periodontitis, a serious form of gum disease.
Active ingredient
Sodium fluoride 0.24%
Child safety
Keep out of reach of children
Inactive ingredient
Inactive Ingredients Water, Silicon Dioxide, Glycerol, Sorbitol, Sodium Lauryl Sulphate, Potassium Citrate Monohydrate, Aroma, Carmellose Sodium, Titanium Dioxide, Tetrasodium Pyrophosphate, Menthol, Cetylpyridinium Chloride, Sodium Benzoate, Sucralose, Methyl Salicylate.

Official sources and product identifiers

Substances listed: SODIUM FLUORIDE

RxNorm identifiers: 416783

Package NDC codes

84035-013-06, 84035-013-50

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.