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United States · US · US:21130-583_e3534cc1-edf9-482f-8462-8d08d36790f3

Tussin DM Cough and Chest Congestion

UNIISPLATC R05DA

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

Identification

ManufacturerSafeway, Inc.
CountryUS (United States)
ATC codeR05DA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    2113058304
    1 BOTTLE, PLASTIC in 1 BOX (21130-583-04) / 118 mL in 1 BOTTLE, PLASTIC
  • ndc11
    2113058308
    1 BOTTLE, PLASTIC in 1 BOX (21130-583-08) / 237 mL in 1 BOTTLE, PLASTIC

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": {
    "e1280355-da81-489f-9bd2-ffea9a68010c": {
      "match": "brand_token",
      "title": "TUSSIN COUGH AND CHEST CONGESTION DM ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [HARRIS TEETER, LLC]",
      "spl_version": "3",
      "published_date": "2026-04-30"
    }
  },
  "productid": "21130-583_e3534cc1-edf9-482f-8462-8d08d36790f3",
  "productndc": "21130-583",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
  "proprietary_name": "Tussin DM Cough and Chest Congestion",
  "active_ingred_unit": "mg/10mL; mg/10mL",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Dextromethorphan HBr, Guaifenesin",
  "start_marketing_date": "20251201",
  "active_numerator_strength": "20; 200"
}

Related drugs

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