Lovita NMN 18000

Manufacturer: ACCOLADE PHARMA USA
Effective date: 2023-06-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 21:30:32

Label at a glance#

ProductLovita NMN 18000

Active ingredientNICOTINAMIDE MONONUCLEOTIDE, RESVERATROL

Label structure1 sections

Label contents#

Full prescribing information#

NMN Nicotinamide Mononucleotide 18000

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Support longevity & anti-aging.

Exclusive formula with resveratrol

NAD+ Precursor

60 Enteric coated vegetarian capsules

Dietary Supplement

20230413-2NMN18000-01-20230419

INSTRUCTIONS FOR USE SECTION

NMN helps boost NAD+ levels in body. NAD+ is required for proper cellular energy utilization and to slow the aging process. Increased NAD+ levels also stimulate SIRTUIN activity.

Recommended storage condition

STORAGE AND HANDLING SECTION

Please refrigerate after opening.

HEALTH CLAIM SECTION

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Lovita NMN 18000
Nicotinamide Monoclueotide
MAGNESIUM STEARATE
NICOTINAMIDE MONONUCLEOTIDE
SILICON DIOXIDE
RESVERATROL
MICROCRYSTALLINE CELLULOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83392-002	83392-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MAGNESIUM STEARATE	70097M6I30	IACT
NICOTINAMIDE MONONUCLEOTIDE	2KG6QX4W0V	ACTIB
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
RESVERATROL	Q369O8926L	ACTIB
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT

Source Document#

Source XML

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ffd9f429-1336-0c2d-e053-6294a90a5372			fd2ba12e-c522-dfa2-e053-6394a90a2802	2023-07-06		Exact identifier spl set id: fd2ba12e-c522-dfa2-e053-6394a90a2802

Reported adverse events (FAERS/openFDA)#

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