GOODSENSE Maximum Strength Medicated

UNIISPL

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

Identification

ManufacturerGEISS, DESTIN & DUNN, INC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5080421148
48 PACKET in 1 PACKAGE (50804-211-48) / 2.9 g in 1 PACKET

Annotations

UNII (FDA Substance ID)

101I4J0U34

WITCH HAZEL

RxCUI 89821

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "101I4J0U34",
    "rxcui": "89821",
    "inchikey": null,
    "display_name": "WITCH HAZEL",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "e42f9e0d-f990-4c33-af43-75acf5d77638": {
      "match": "brand_token",
      "title": "GOODSENSE COMBO PACK DAYTIME AND NIGHTTIME (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [L. PERRIGO COMPANY]",
      "spl_version": "1",
      "published_date": "2026-05-21"
    }
  },
  "productid": "50804-211_453a56d2-cd45-a854-e063-6394a90a969d",
  "productndc": "50804-211",
  "dosage_form": "CLOTH",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WITCH HAZEL",
  "proprietary_name": "GOODSENSE Maximum Strength Medicated",
  "active_ingred_unit": "g/100g",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "WITCH HAZEL",
  "start_marketing_date": "20170727",
  "active_numerator_strength": "50"
}

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