NDC 71894-110 - Zolgensma

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 71894-110
Package NDCs from labels: 71894-110-01
Manufacturer: Novartis Innovative Technologies Inc.
Effective date: 2026-06-16
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Zolgensma - Novartis Innovative Technologies Inc.	Novartis Innovative Technologies Inc.	2026-06-16	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	11.0 mL	20000000000000 [arb'U] in 1mL	14
71894-110-01	Zolgensma	5.5 mL in 1 VIAL	INJECTION, SUSPENSION	5.5 mL	20000000000000 [arb'U] in 1mL	14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71894-110	ZOLGENSMA (ONASEMNOGENE ABEPARVOVEC-XIOI) KIT [NOVARTIS GENE THERAPIES, INC.]	13	Unmatched	20250214_68cd4f06-70e1-40d8-bedb-609ec0afa471.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 18 of 89 · 1,774 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
70% Isopropyl Rubbing Alcohol	ISOPROPYL RUBBING ALCOHOL	Better Living Brands, LLC	4817df03-05a2-4e85-bec2-a06f9d57d0b8	2026-02-24	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Better Living Brands, LLC	4031ea5d-cba4-44f5-9a81-0cab2367d97e	2026-02-24	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Better Living Brands, LLC	6391432a-a5b8-4528-88a6-862bc2062f68	2026-02-24	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Isopropyl	ISOPROPYL ALCOHOL	H E B	25fea857-9ed8-49e7-b892-b24f639f83ca	2026-02-24	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
70%	ISOPROPYL ALCOHOL	H E B	403e52e8-bac1-460a-81ef-bac5a7b5de10	2026-02-24	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Isopropyl Alcohol	ISOPROPYL ALCOHOL	H E B	28cd16f5-61c5-4943-9dd6-a9864fa35806	2026-02-24	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
50% Isopropyl Alcohol	ISOPROPYL ALCOHOL	H E B	0ed762dd-9432-45b4-9e75-c24fb28ff956	2026-02-24	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Sunvine 70 Isopropyl Alcohol First Aid Antiseptic	ISOPROPYL ALCOHOL	Mac Innovations, LLC	8435ef45-5d2c-4bbb-b9e0-0b00c1ec8c76	2026-02-24	Warnings	Exact identifier unii: ND2M416302
Alcohol Prep Pads	ISOPROPYL ALCOHOL	ALCOVE BRANDS	4bad1fee-b4fe-c518-e063-6294a90a0318	2026-02-24	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
BM BIO28 (General Tonic)	CALC SULPH, CALC FLUOR, CALC PHOS, FERR PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT PHOS, NAT SULPH, NAT MUR, SILICEA	BM Private Limited	38d2cff0-3550-b119-e063-6394a90a31cb	2026-02-23	Warnings	Exact identifier unii: 451W47IQ8X
Isopropyl Rubbing Alcohol	ISOPROPYL ALCOHOL	4 Visions LLC	4b87d4cc-163e-1432-e063-6294a90af483	2026-02-23	Warnings	Exact identifier unii: ND2M416302
Isopropyl Alcohol	ISOPROPYL ALCOHOL	4 Visions LLC	4b88008f-fe78-4b7e-e063-6294a90ab9ae	2026-02-23	Warnings	Exact identifier unii: ND2M416302
Universal Rubbing Alcohol	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	183efdc2-cf3e-4f06-b292-0cfd097418b3	2026-02-23	Warnings	Exact identifier unii: ND2M416302
Allergy Kids	URTICA DIOICA LEAF, INULA HELENIUM ROOT, ANGELICA ARCHANGELICA ROOT, PINE NEEDLE OIL (PINUS SYLVESTRIS), SODIUM CHLORIDE, AND ALTHAEA OFFICINALIS ROOT	Forces of Nature	4886109c-dd7d-40c0-911f-5f12343d8e63	2026-02-20	Warnings	Exact identifier unii: 451W47IQ8X
Allergy Maximum Strength	URTICA DIOICA, ALTHAEA OFFICINALIS ROOT, INULA HELENIUM ROOT, ANGELICA ARCHANGELICA ROOT, PINE NEEDLE OIL (PINUS SYLVESTRIS), SODIUM CHLORIDE, AND SILICON DIOXIDE	Forces of Nature	122ca23e-43f1-4e5c-afc2-1418b1717679	2026-02-20	Warnings	Exact identifier unii: 451W47IQ8X
Back Pain Pain Management	ARNICA MONTANA, HORSE CHESTNUT, HYPERICUM PERFORATUM, RUTA GRAVEOLENS WHOLE, AND SODIUM CHLORIDE	Forces of Nature	bf089347-f334-4d6d-ab58-cf7f0b16810f	2026-02-20	Warnings	Exact identifier unii: 451W47IQ8X
PDI Alcohol Prep Pad Sterile Large and Medium	ALCOHOL	Professional Disposables International Inc	8fe9cf1c-3f5f-4873-9648-6d4c79f8cf03	2026-02-18	Warnings	Exact identifier rxcui: 797544
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Target Corporation	b5455e53-2b86-48e7-a479-664f6601bab7	2026-02-18	Warnings, Adverse reactions	Exact identifier unii: ND2M416302
Travel Wipes Unscented	ISOPROPYL ALCOHOL	SINGULAR ENTERPRISES LLC	dd046146-fda7-438c-98ca-96ea1dd0ae0b	2026-02-18	Warnings	Exact identifier rxcui: 797544 unii: ND2M416302
70%	ISOPROPYL ALCOHOL	Target Corporation	4db7c9cb-021d-463a-9ff6-91ae42f0311d	2026-02-18	Warnings, Adverse reactions	Exact identifier unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.