Tukol Multi Symptom Cold

UNIISPLATC R05DA

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

Identification

ManufacturerGenomma Lab USA, Inc.

CountryUS (United States)

ATC codeR05DA

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5006650424
118 mL in 1 BOTTLE (50066-504-24)

Annotations

UNII (FDA Substance ID)

9D2RTI9KYH

DEXTROMETHORPHAN HYDROBROMIDE

RxCUI 102490

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "9D2RTI9KYH",
    "rxcui": "102490",
    "inchikey": "STTADZBLEUMJRG-IKNOHUQMSA-N",
    "display_name": "DEXTROMETHORPHAN HYDROBROMIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "73358103-43dc-4b11-9c89-9a6ba45bf1af": {
      "match": "brand_token",
      "title": "TUKOL MAX ACTION (OXYMETAZOLINE HYDROCHLORIDE) LIQUID [GENOMMA LAB USA]",
      "spl_version": "1",
      "published_date": "2025-02-17"
    }
  },
  "productid": "50066-504_4c7fab8b-ba17-4210-9f16-05fdac6cf62b",
  "productndc": "50066-504",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
  "proprietary_name": "Tukol Multi Symptom Cold",
  "active_ingred_unit": "mg/5mL; mg/5mL; mg/5mL",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE",
  "start_marketing_date": "20120515",
  "active_numerator_strength": "10; 100; 5"
}

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