NDC 86157-0001 - PROVETI DENTI PREMIUM

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: 86157-0001
Package NDCs from labels: 86157-0001-1
Manufacturer: SUN LIFE SCIENCE Co.,Ltd. | PL COSMETIC
Effective date: 2022-03-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PROVETI DENTI PREMIUM - SUN LIFE SCIENCE Co.,Ltd. \| PL COSMETIC	SUN LIFE SCIENCE Co.,Ltd. \| PL COSMETIC	2022-03-08	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
86157-0001-1	PROVETI DENTI PREMIUM	50 mL in 1 BOTTLE, SPRAY	LIQUID	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
86157-0001	PROVETI DENTI PREMIUM (POTASSIUM CARBONATE) LIQUID [SUN LIFE SCIENCE CO.,LTD.]	1	1 package rows	20220315_92d9d85a-3af3-4c09-a08c-817161e81ff5.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 10 of 10 · 181 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

Reported adverse events (FAERS/openFDA)#

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