Rohto

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerThe Mentholatum Company

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
1074281611
30 VIAL, SINGLE-USE in 1 CARTON (10742-8161-1) / .5 mL in 1 VIAL, SINGLE-USE

Annotations

UNII (FDA Substance ID)

FZ989GH94E

POVIDONE, UNSPECIFIED

RxCUI 8610

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "FZ989GH94E",
    "rxcui": "8610",
    "inchikey": null,
    "display_name": "POVIDONE, UNSPECIFIED",
    "substance_type": "mixture",
    "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": "10742-8161_29790c01-f34c-a19a-e063-6294a90aa5a0",
  "productndc": "10742-8161",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "POVIDONE, UNSPECIFIED; PROPYLENE GLYCOL",
  "proprietary_name": "Rohto",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "povidone, propylene glycol",
  "start_marketing_date": "20220603",
  "active_numerator_strength": "6.8; 3"
}

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