NDC 51688-6485 - A4172 NERVE BLOCK

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: 51688-6485
Package NDCs from labels: 51688-6485-2
Manufacturer: Smiths Medical ASD, Inc. | Hospira, Inc.
Effective date: 2015-03-24
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
A4172 NERVE BLOCK - Smiths Medical ASD, Inc. \| Hospira, Inc.	Smiths Medical ASD, Inc. \| Hospira, Inc.	2015-03-24	MEDICAL DEVICE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
LIDOCAINE HYDROCHLORIDE	ACTIVE INGREDIENT	V13007Z41A	A4172 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]	1
SODIUM CHLORIDE	ACTIVE INGREDIENT	451W47IQ8X	A4172 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]	1
Lidocaine	ACTIVE MOIETY	98PI200987	A4172 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]	1
SODIUM CATION	ACTIVE MOIETY	LYR4M0NH37	A4172 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]	1
Hydrochloric Acid	INACTIVE INGREDIENT	QTT17582CB	A4172 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]	1
Sodium Chloride	INACTIVE INGREDIENT	451W47IQ8X	A4172 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]	1
Sodium Hydroxide	INACTIVE INGREDIENT	55X04QC32I	A4172 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	A4172 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]	1

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 83 of 83 · 1,646 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Sodium Chloride	SODIUM CHLORIDE	Baxter Healthcare Corporation	2a96096d-43cc-49b7-af53-b53c17f41001	2014-07-25	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
SODIUM CHLORIDE	SODIUM CHLORIDE	Baxter Healthcare Corporation	b3b4b176-41f0-4ca8-90d4-3fba5707564a	2014-02-21		Exact identifier unii: 451W47IQ8X
TIS-U-SOL	SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE	Baxter Healthcare Corporation	9da4121f-d62d-4da4-8dfb-0494da16015f	2014-02-21		Exact identifier unii: 451W47IQ8X
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,	Baxter Healthcare Corporation	e1953d54-818d-46a6-8532-518ebae6d84e	2012-06-13		Exact identifier unii: 451W47IQ8X
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12		Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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