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CrystLCare Regeneration Plus drug information

POTASSIUM NITRATE, SODIUM FLUORIDE
GreenMark Biomedical Inc. · ORAL

Product NDC: 87587-250

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic namePOTASSIUM NITRATE, SODIUM FLUORIDE
Labeler / manufacturerGreenMark Biomedical Inc.
RouteORAL
Drug classDrug class not supplied in source label
Product NDC87587-250
Label effective date2026-09-14

Official product label reference

CrystLCare Regeneration Plus — GreenMark Biomedical Inc.

This page contains 8 source sections for POTASSIUM NITRATE, SODIUM FLUORIDE, oral route. Label set 4f86d0a0-d73e-5605-e063-6394a90adb38, version 1.

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

USES Aids in the prevention of dental caries (cavities) Builds protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact

Purpose

PURPOSE Antisensitivity Anticavity
Dosage and administration — label text
DIRECTIONS adults and children 6 years of age and older: Use once a day after brushing teeth with toothpaste followed by rinsing with water. Apply dental strip onto the teeth. Allow to remain on the teeth for 3 min and then spit out residue. Do not eat or drink for 30 minutes. Instruct children under 12 years of age in the use of this product. Supervise children as necessary until capable of using without supervision. children under the age of 6: Consult a dentist.
Warnings
WARNINGS For topical intraoral use only. 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 for more than 4 weeks unless recommended by a dentist or doctor.
Active ingredient
ACTIVE INGREDIENTS Potassium Nitrate 5% Sodium Fluoride 0.05%
Child safety
Keep out of reach of children. If more than used for daily application is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Inactive ingredient
INACTIVE INGREDIENT SECTION Calcium/phosphate loaded starch particle (contains Calcium, Phosphate, Starch), natural peppermint oil, pullulan, stevia, vegetable glycerin, water.
Questions
QUESTIONS 1-810-899-0710

Official sources and product identifiers

Substances listed: POTASSIUM NITRATE, SODIUM FLUORIDE

Package NDC codes

87587-250-50, 87587-250-01

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.