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United States · US · US:51206-308_43d0f364-2387-9fae-e063-6394a90a4777
Opalescence Sensitivity Relief Whitening
In shortageUNIISPLATC C03CB
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUltradent Products, Inc.
CountryUS (United States)
ATC codeC03CB
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc1151206308011 TUBE in 1 CARTON (51206-308-01) / 28.35 g in 1 TUBE
- ndc1151206308021 TUBE in 1 CARTON (51206-308-02) / 133 g in 1 TUBE
- ndc1151206308033 CARTON in 1 PACKAGE, COMBINATION (51206-308-03) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
- ndc11512063080412 CARTON in 1 PACKAGE, COMBINATION (51206-308-04) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
- ndc11512063080524 CARTON in 1 PACKAGE, COMBINATION (51206-308-05) / 1 TUBE in 1 CARTON / 28.35 g in 1 TUBE
- ndc1151206308066 CARTON in 1 PACKAGE, COMBINATION (51206-308-06) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
RU45X2JN0Z
POTASSIUM NITRATE
RxCUI 34316
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Potassium Citrate Tablet, Extended Release
Raw payload (JSON)
{
"unii": {
"unii": "RU45X2JN0Z",
"rxcui": "34316",
"inchikey": "FGIUAXJPYTZDNR-UHFFFAOYSA-N",
"display_name": "POTASSIUM NITRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "DENTAL",
"spl_meta": {
"44e7d0ed-3c37-5889-e063-6294a90afcca": {
"match": "brand_token",
"title": "OPALESCENCE WHITENING COOL MINT (SODIUM FLUORIDE) GEL, DENTIFRICE [ULTRADENT PRODUCTS, INC.]",
"spl_version": "3",
"published_date": "2026-04-08"
}
},
"productid": "51206-308_43d0f364-2387-9fae-e063-6394a90a4777",
"productndc": "51206-308",
"dosage_form": "GEL, DENTIFRICE",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "POTASSIUM NITRATE; SODIUM FLUORIDE",
"shortage_reason": "Potassium Citrate Tablet, Extended Release",
"shortage_status": "current",
"proprietary_name": "Opalescence Sensitivity Relief Whitening",
"active_ingred_unit": "mg/g; mg/g",
"application_number": "M022",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Potassium Nitrate and Sodium Fluoride",
"start_marketing_date": "20151130",
"active_numerator_strength": "50; 1.1"
}Related drugs
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