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United States · US · US:66613-8459_29ab2269-62a8-00b9-e063-6394a90aaf5b

Rohto

UNIISPLATC S01KA

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerRohto Pharmaceutical Co., Ltd.
CountryUS (United States)
ATC codeS01KA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6661384591
    1 BOTTLE, DISPENSING in 1 CARTON (66613-8459-1) / 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": "66613-8459_29ab2269-62a8-00b9-e063-6394a90aaf5b",
  "productndc": "66613-8459",
  "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

Other records sharing ATC code S01KA.

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