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United States · US · US:59883-020_82f8eacb-a214-3080-e053-2a91aa0a6a07
FLUORIDEX
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
- ndc1159883020041 TUBE in 1 BOX (59883-020-04) / 112 g in 1 TUBE
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": "DENTAL",
"spl_meta": {
"601774d5-f4de-01bc-e053-2991aa0a7f4f": {
"match": "brand_token",
"title": "FLUORIDEX (SODIUM FLUORIDE) PASTE, DENTIFRICE [DENT-MAT HOLDINGS, LLC.]",
"spl_version": "5",
"published_date": "2025-01-31"
}
},
"productid": "59883-020_82f8eacb-a214-3080-e053-2a91aa0a6a07",
"productndc": "59883-020",
"dosage_form": "PASTE, DENTIFRICE",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SODIUM FLUORIDE",
"shortage_reason": "Sodium Acetate Injection",
"shortage_status": "current",
"proprietary_name": "FLUORIDEX",
"active_ingred_unit": "mg/g",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "Sodium Fluoride",
"start_marketing_date": "20170103",
"active_numerator_strength": "5"
}Related drugs
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