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United States · US · US:10742-8146_2978e2bc-c901-60bb-e063-6394a90a47a7

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

  • ndc11
    1074281461
    1 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8146-1) / 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": "10742-8146_2978e2bc-c901-60bb-e063-6394a90a47a7",
  "productndc": "10742-8146",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HYPROMELLOSE, UNSPECIFIED; TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE, UNSPECIFIED FORM",
  "proprietary_name": "Rohto",
  "active_ingred_unit": "mg/mL; mg/mL; mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Hypromellose, Tetrahydrozoline hydrochloride, Zinc sulfate",
  "start_marketing_date": "20210621",
  "active_numerator_strength": "2; .5; 2.5"
}

Related drugs

Other records sharing ATC code S01KA.

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