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United States · US · US:82584-700_4197af7c-fb98-684b-e063-6394a90a64cf
iVIZIA Dry Eye
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerThea Pharma Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1182584700051 BOTTLE, DROPPER in 1 CARTON (82584-700-05) / 5 mL in 1 BOTTLE, DROPPER
- ndc1182584700111 BOTTLE, DROPPER in 1 CARTON (82584-700-11) / 10 mL in 1 BOTTLE, DROPPER
- ndc1182584700131 BOTTLE, DROPPER in 1 CARTON (82584-700-13) / 5 mL in 1 BOTTLE, DROPPER
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "OPHTHALMIC",
"spl_meta": {
"1f06ca1a-5270-9a82-e063-6294a90aed64": {
"match": "brand_token",
"title": "IVIZIA LUBRICANT EYE GEL (POVIDONE) GEL [THEA PHARMA INC.]",
"spl_version": "3",
"published_date": "2026-05-04"
}
},
"productid": "82584-700_4197af7c-fb98-684b-e063-6394a90a64cf",
"productndc": "82584-700",
"dosage_form": "SOLUTION/ DROPS",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "POVIDONE",
"proprietary_name": "iVIZIA Dry Eye",
"active_ingred_unit": "mg/5mL",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "povidone",
"start_marketing_date": "20241201",
"active_numerator_strength": "25"
}Access this data programmatically
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