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United States · US · US:61354-119_3e142cd6-160d-62f8-e063-6394a90ae70c
Powder
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerOxygen Development LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1161354119021 CUP in 1 CARTON (61354-119-02) / 100 mg in 1 CUP (61354-119-01)
Annotations
UNII (FDA Substance ID)
1K09F3G675
FERRIC OXIDE RED
RxCUI 1310572
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "1K09F3G675",
"rxcui": "1310572",
"inchikey": "LIKBJVNGSGBSGK-UHFFFAOYSA-N",
"display_name": "FERRIC OXIDE RED",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"41c0c262-21c3-b8e6-e063-6394a90a7c9c": {
"match": "brand_token",
"title": "POWDER (TITANIUM DIOXIDE) POWDER [OXYGEN DEVELOPMENT LLC]",
"spl_version": "4",
"published_date": "2026-03-18"
}
},
"productid": "61354-119_3e142cd6-160d-62f8-e063-6394a90ae70c",
"productndc": "61354-119",
"dosage_form": "POWDER",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "FERRIC OXIDE RED; TITANIUM DIOXIDE",
"proprietary_name": "Powder",
"active_ingred_unit": "mg/100mg; mg/100mg",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Titanium Dioxide",
"start_marketing_date": "20231027",
"active_numerator_strength": "1.75; 10"
}Access this data programmatically
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