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United States · US · US:0023-9232_265710db-c7b9-42ff-9fc8-c24a936c1d87
BOTOX Cosmetic
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllergan, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 0
No packs registered.
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": "0023-9232_265710db-c7b9-42ff-9fc8-c24a936c1d87",
"productndc": "0023-9232",
"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": "20080520",
"active_numerator_strength": "100"
}Access this data programmatically
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