Lumavex

Product NDC
85477-610
Requested package NDC
85477-610-30
11-digit product format
854770610
Labeler code
85477
Product ID
85477-610_4139742d-d090-121c-e063-6394a90a6221
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Multivitamin
Dosage form
CAPSULE
Route
ORAL
Labeler
Oncora Pharma, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2025-10-15
Substance
ASCORBIC ACID; FOLIC ACID; METHYLCOBALAMIN; NIACINAMIDE; PANTOTHENIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE
Active strength
65; 1.67; .5; 35.7; 20; 25; 5; 5 mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
Pharmacologic classes
Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Lumavex
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
THIAMINE HYDROCHLORIDE65 mg/1
NIACINAMIDE1.67 mg/1
PYRIDOXINE HYDROCHLORIDE.5 mg/1
ASCORBIC ACID35.7 mg/1
PANTOTHENIC ACID20 mg/1
RIBOFLAVIN25 mg/1
FOLIC ACID5 mg/1
METHYLCOBALAMIN5 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
M572600E5PInternal UNII lookup
25X51I8RD4Internal UNII lookup
68Y4CF58BVInternal UNII lookup
PQ6CK8PD0RInternal UNII lookup
19F5HK2737Internal UNII lookup
TLM2976OFRInternal UNII lookup
935E97BOY8Internal UNII lookup
BR1SN1JS2WInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4139742d-d091-121c-e063-6394a90a6221Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cf050ccd-1144-f76a-e00d-e5698d8597d4Product name620250625
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
91c62db0-0295-c81c-d10a-0856c259edd6Product name220200428
d32bc2b8-0bb7-2216-87aa-24639646e202Product name320190619
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
5e18e798-5614-cf5c-0185-38b1cb77a093Product name220160822

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85477-610-30Lumavex30 in 1 BOTTLECAPSULE301

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LumavexMULTIVITAMINOncora Pharma, LLC4139742d-d091-121c-e063-6394a90a62212025-10-15Warnings, Adverse reactionsExact identifier
ndc (package): 85477-610-30
ndc (product): 85477-610
ndc11 (package): 85477061030

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85477-610-308547706103030 CAPSULE in 1 BOTTLE (85477-610-30) 30 capsule2025-10-15NoNoCurrent