NDC 84781-102 - FLORASTART

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: 84781-102
Package NDCs from labels: 84781-102-01
Manufacturer: Trivia Pharmaceuticals, LLC
Effective date: 2025-02-05
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
FLORASTART - Trivia Pharmaceuticals, LLC	Trivia Pharmaceuticals, LLC	2025-02-05	DIETARY SUPPLEMENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84781-102-01	FLORASTART	30 in 1 BOTTLE	CAPSULE	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84781-102	FLORASTART (SACCHAROMYCES BOULARDII) CAPSULE [TRIVIA PHARMACEUTICALS, LLC]	1	1 package rows	20250207_bb7e1a2e-fbff-454f-8163-081879a5d80b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
84781-102-01	EA - Each	84781-102	588b0034-120b-498f-b4d2-6f95f36a3f7a	1	2025-03-04

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
Aspartame/MSG Detox	CHELIDONIUM MAJUS, ARNICA MONTANA, PHYTOLACCA DECANDRA, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM, BISPHENOL A (BPA), DEXTROSE, MALTODEXTRIN, SUCRALOSE, ASPARTIC ACID, DIKETOPIPERAZINE, DOPAMINE HYDROCHLORIDE, FORMALINUM, FORMICUM ACIDUM, L-PHENYLALANINE, METHYL ALCOHOL, MONOSODIUM GLUTAMATE	Deseret Biologicals, Inc.	a1dc1bf3-db71-4550-a975-4f146fb94005	2025-03-11	Warnings	Exact identifier unii: 7CVR7L4A2D

Reported adverse events (FAERS/openFDA)#

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