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United States · US · US:63868-235_4f7077f9-5790-46dd-88dc-236cd702e250

Mucus Relief DM Max

UNIISPLATC R05DA

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

Identification

ManufacturerQUALITY CHOICE (Chain Drug Marketing Association)
CountryUS (United States)
ATC codeR05DA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6386823506
    177 mL in 1 BOTTLE, PLASTIC (63868-235-06)

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": {
    "84b5d83d-aea5-42ed-b20c-96d3b389c8c0": {
      "match": "brand_token",
      "title": "MUCUS RELIEF DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) TABLET, EXTENDED RELEASE [RITE AID CORPORATION]",
      "spl_version": "3",
      "published_date": "2026-05-28"
    }
  },
  "productid": "63868-235_4f7077f9-5790-46dd-88dc-236cd702e250",
  "productndc": "63868-235",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
  "proprietary_name": "Mucus Relief DM Max",
  "active_ingred_unit": "mg/20mL; mg/20mL",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Dextromethorphan HBr, Guaifenesin",
  "start_marketing_date": "20160331",
  "active_numerator_strength": "20; 400"
}

Related drugs

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