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United States · US · US:82442-384_f1856542-23c1-48ca-921a-62d9b42ac5a8

up and up Medicated Anti-dandruff

UNIISPLATC D01AE13

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

Identification

ManufacturerTARGET CORPORATION
CountryUS (United States)
ATC codeD01AE13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    8244238401
    355 mL in 1 BOTTLE (82442-384-01)

Annotations

UNII (FDA Substance ID)
Z69D9E381Q
SELENIUM SULFIDE
RxCUI 36345
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "Z69D9E381Q",
    "rxcui": "36345",
    "inchikey": "JNMWHTHYDQTDQZ-UHFFFAOYSA-N",
    "display_name": "SELENIUM SULFIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "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": "82442-384_f1856542-23c1-48ca-921a-62d9b42ac5a8",
  "productndc": "82442-384",
  "dosage_form": "SHAMPOO",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SELENIUM SULFIDE",
  "proprietary_name": "up and up Medicated Anti-dandruff",
  "active_ingred_unit": "mg/mL",
  "application_number": "M032",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "SELENIUM SULFIDE",
  "start_marketing_date": "20240404",
  "active_numerator_strength": "10"
}

Related drugs

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