NDC 59282-108 - Encore Activator

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: 59282-108
Package NDCs from labels: 59282-108-17, 59282-108-21
Manufacturer: ABS Global Inc.
Effective date: 2021-10-28
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Encore Activator - ABS Global Inc.	ABS Global Inc.	2021-10-28	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59282-108-17	Encore Activator	56780 mL in 1 DRUM	SOLUTION	56780		4
59282-108-21	Encore Activator	208200 mL in 1 DRUM	SOLUTION	208200		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59282-108	ENCORE ACTIVATOR (CHLORUS ACID) SOLUTION [ABS GLOBAL INC.]	4	2 package rows	20211030_36866edb-96b8-4265-99a8-4f4fb5ee17fb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CHLOROUS ACID	ACTIVE INGREDIENT	7JRT833T5M	ENCORE ACTIVATOR (CHLORUS ACID) SOLUTION [ABS GLOBAL INC.]	1
CHLOROUS ACID	ACTIVE MOIETY	7JRT833T5M	ENCORE ACTIVATOR (CHLORUS ACID) SOLUTION [ABS GLOBAL INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ENCORE ACTIVATOR (CHLORUS ACID) SOLUTION [ABS GLOBAL 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 9 of 9 · 161 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.