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United States · US · US:59883-920_82f8dd55-36df-0de0-e053-2991aa0a6bbf
Pro-Den Rx
In shortageUNIISPLATC A01AA51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDen-mat Holdings, Llc
CountryUS (United States)
ATC codeA01AA51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc115988392016473 mL in 1 BOTTLE, PLASTIC (59883-920-16)
Annotations
UNII (FDA Substance ID)
8ZYQ1474W7
SODIUM FLUORIDE
RxCUI 9873
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Sodium Acetate Injection
Raw payload (JSON)
{
"unii": {
"unii": "8ZYQ1474W7",
"rxcui": "9873",
"inchikey": "PUZPDOWCWNUUKD-UHFFFAOYSA-M",
"display_name": "SODIUM FLUORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"9036aa8a-59b1-41b0-b3cb-529d3303a1c0": {
"match": "brand_token",
"title": "PRO-DEN RX (STANNOUS FLUORIDE) RINSE [DEN-MAT HOLDINGS, LLC]",
"spl_version": "6",
"published_date": "2023-12-18"
}
},
"productid": "59883-920_82f8dd55-36df-0de0-e053-2991aa0a6bbf",
"productndc": "59883-920",
"dosage_form": "RINSE",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SODIUM FLUORIDE",
"shortage_reason": "Sodium Acetate Injection",
"shortage_status": "current",
"proprietary_name": "Pro-Den Rx",
"active_ingred_unit": "mg/mL",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "Sodium Fluoride",
"start_marketing_date": "20081021",
"active_numerator_strength": ".9"
}Related drugs
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