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United States · US · US:72960-112_71c76e28-0eb6-487e-a53b-4c9e78021e57
DAXXIFY
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRevance Therapeutics, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1172960112011 VIAL, SINGLE-USE in 1 CARTON (72960-112-01) / 1.2 mL in 1 VIAL, SINGLE-USE
- ndc1172960112021 VIAL, SINGLE-USE in 1 CARTON (72960-112-02) / 1.2 mL in 1 VIAL, SINGLE-USE
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": {
"3aaa6e14-a3f7-4fb2-b9f9-d3a9c3ae1f74": {
"match": "brand_token",
"title": "DAXXIFY (BOTULINUM TOXIN TYPE A) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [REVANCE THERAPEUTICS, INC.]",
"spl_version": "12",
"published_date": "2026-01-08"
}
},
"productid": "72960-112_71c76e28-0eb6-487e-a53b-4c9e78021e57",
"productndc": "72960-112",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BOTULINUM TOXIN TYPE A",
"proprietary_name": "DAXXIFY",
"active_ingred_unit": "U/1.2mL",
"application_number": "BLA761127",
"marketing_category": "BLA",
"nonproprietary_name": "botulinum toxin type A",
"start_marketing_date": "20220920",
"active_numerator_strength": "100"
}Access this data programmatically
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