UP and UP Daytime Childrens Multi Symptom Cold

UNIISPLATC R05DA

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

Identification

ManufacturerTarget Corporation

CountryUS (United States)

ATC codeR05DA

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8244269404
1 BOTTLE in 1 CARTON (82442-694-04) / 118 mL in 1 BOTTLE

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": {
    "51c0a953-93cb-4d0a-b51c-02d9482d1746": {
      "match": "brand_token",
      "title": "UP AND UP ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [TARGET CORPORATION]",
      "spl_version": "12",
      "published_date": "2026-05-13"
    }
  },
  "productid": "82442-694_42d7a5e8-c8bb-0e3f-e063-6294a90a7c4c",
  "productndc": "82442-694",
  "dosage_form": "SUSPENSION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
  "proprietary_name": "UP and UP Daytime Childrens 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, and Phenylephrine Hydrochloride",
  "start_marketing_date": "20240719",
  "active_numerator_strength": "5; 100; 2.5"
}

Related drugs

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