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United States · US · US:10742-8459_29aaa211-07f2-71e1-e063-6294a90a1e43
Rohto
UNIISPLATC S01KA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerThe Mentholatum Company
CountryUS (United States)
ATC codeS01KA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1110742845911 BOTTLE, DISPENSING in 1 CARTON (10742-8459-1) / 18 mL in 1 BOTTLE, DISPENSING
Annotations
UNII (FDA Substance ID)
3NXW29V3WO
HYPROMELLOSE, UNSPECIFIED
RxCUI 27334
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3NXW29V3WO",
"rxcui": "27334",
"inchikey": null,
"display_name": "HYPROMELLOSE, UNSPECIFIED",
"substance_type": "polymer",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "OPHTHALMIC",
"spl_meta": {
"1b597f83-d7f1-cf93-e063-6394a90a99f7": {
"match": "brand_token",
"title": "ROHTO DUAL LIGHT RELIEF (HYPROMELLOSE, POVIDONE) LIQUID [THE MENTHOLATUM COMPANY]",
"spl_version": "3",
"published_date": "2024-12-23"
}
},
"productid": "10742-8459_29aaa211-07f2-71e1-e063-6294a90a1e43",
"productndc": "10742-8459",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "HYPROMELLOSE, UNSPECIFIED; POVIDONE",
"proprietary_name": "Rohto",
"active_ingred_unit": "mg/mL; mg/mL",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Hypromellose, Povidone",
"start_marketing_date": "20240530",
"active_numerator_strength": "3; 5"
}Related drugs
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