BOTOX Cosmetic

UNIISPL

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

Identification

ManufacturerAllergan, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
0023391950
1 VIAL, GLASS in 1 CARTON (0023-3919-50) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS
ndc11
0023391951
1 VIAL, GLASS in 1 CARTON (0023-3919-51) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS

Annotations

UNII (FDA Substance ID)

E211KPY694

BOTULINUM TOXIN TYPE A

RxCUI 1712

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "E211KPY694",
    "rxcui": "1712",
    "inchikey": null,
    "display_name": "BOTULINUM TOXIN TYPE A",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAMUSCULAR",
  "spl_meta": {
    "a6f42753-d31e-4b23-8da0-4b990fee4b38": {
      "match": "brand_token",
      "title": "BOTOX (ONABOTULINUMTOXINA) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SPORTPHARM LLC]",
      "spl_version": "1",
      "published_date": "2026-02-06"
    }
  },
  "productid": "0023-3919_265710db-c7b9-42ff-9fc8-c24a936c1d87",
  "productndc": "0023-3919",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BOTULINUM TOXIN TYPE A",
  "proprietary_name": "BOTOX Cosmetic",
  "active_ingred_unit": "[USP'U]/1",
  "application_number": "BLA103000",
  "marketing_category": "BLA",
  "nonproprietary_name": "onabotulinumtoxinA",
  "start_marketing_date": "20080715",
  "active_numerator_strength": "50"
}

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