🇺🇸
United States · US · US:73242-1120_4119a974-5d1d-c809-e063-6294a90a635d
DENTI BUONGIORNO ORIGINAL TOOTH
UNIISPLATC A01AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDONG IL PHARMS CO.,LTD
CountryUS (United States)
ATC codeA01AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1173242112021 TUBE in 1 CARTON (73242-1120-2) / 100 g in 1 TUBE (73242-1120-1)
Annotations
UNII (FDA Substance ID)
ETJ7Z6XBU4
SILICON DIOXIDE
RxCUI 9771
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "ETJ7Z6XBU4",
"rxcui": "9771",
"inchikey": "VYPSYNLAJGMNEJ-UHFFFAOYSA-N",
"display_name": "SILICON DIOXIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"487cd5b9-28f3-392d-e063-6394a90a9ba1": {
"match": "brand_token",
"title": "DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH (SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE) PASTE, DENTIFRICE [DONG IL PHARMS CO.,LTD]",
"spl_version": "1",
"published_date": "2026-01-19"
}
},
"productid": "73242-1120_4119a974-5d1d-c809-e063-6294a90a635d",
"productndc": "73242-1120",
"dosage_form": "PASTE, DENTIFRICE",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE",
"proprietary_name": "DENTI BUONGIORNO ORIGINAL TOOTH",
"active_ingred_unit": "g/100g; g/100g",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "Silica, Sodium Monofluorophosphate",
"start_marketing_date": "20250401",
"active_numerator_strength": "18; .76"
}Related drugs
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