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United States · US · US:10742-8175_29791cca-8e12-8094-e063-6394a90a863c
Rohto Digi-Eye
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
- ndc1110742817511 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8175-1) / 13 mL in 1 BOTTLE, WITH APPLICATOR
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": "10742-8175_29791cca-8e12-8094-e063-6394a90a863c",
"productndc": "10742-8175",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "HYPROMELLOSE, UNSPECIFIED; TETRAHYDROZOLINE HYDROCHLORIDE",
"proprietary_name": "Rohto Digi-Eye",
"active_ingred_unit": "mg/mL; mg/mL",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Hypromellose, Tetrahydrozoline hydrochloride",
"start_marketing_date": "20180301",
"active_numerator_strength": "3.5; .5"
}Related drugs
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