NDC 47682-230-18 - Medi-First Cold Spray

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: 47682-230
Requested NDC: 47682-230-18
Package NDCs from labels: 47682-230-18
Manufacturer: Unifirst First Aid Corporation
Effective date: 2013-04-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Medi-First Cold Spray - Unifirst First Aid Corporation	Unifirst First Aid Corporation	2013-04-10	OTC MEDICAL DEVICE LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
47682-230-18	Medi-First Cold Spray	113 g in 1 BOTTLE, SPRAY		113		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
47682-230	MEDI-FIRST COLD SPRAY () [UNIFIRST FIRST AID CORPORATION]	1	1 package rows	20130417_12dee3e7-ffe7-47e1-b258-544f464b9e35.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Toxagent Detox 6035	TOXAGENT DETOX	Professional Complementary Health Formulas	e1476ce1-32ff-4c25-a330-dc78908f5591	2026-01-08	Warnings	Exact identifier unii: T75W9911L6

Reported adverse events (FAERS/openFDA)#

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