NDC 47082-411 - CLEAN EYES

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
47082-411
Package NDCs from labels
47082-411-04
Manufacturer
WESTWOOD LABORATORIES INC.
Effective date
2020-12-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
CLEAN EYESWESTWOOD LABORATORIES INC.2020-12-28OTC ANIMAL DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
WATERACTIVE INGREDIENT059QF0KO0RCLEAN EYES IRRIGANT [WESTWOOD LABORATORIES INC.]2
WATERACTIVE MOIETY059QF0KO0RCLEAN EYES IRRIGANT [WESTWOOD LABORATORIES INC.]2
BORIC ACIDINACTIVE INGREDIENTR57ZHV85D4CLEAN EYES IRRIGANT [WESTWOOD LABORATORIES INC.]2
COBALT DISODIUM EDETATEINACTIVE INGREDIENT3EY1Y2QRLICLEAN EYES IRRIGANT [WESTWOOD LABORATORIES INC.]2
SODIUM BORATEINACTIVE INGREDIENT91MBZ8H3QOCLEAN EYES IRRIGANT [WESTWOOD LABORATORIES INC.]2
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XCLEAN EYES IRRIGANT [WESTWOOD LABORATORIES INC.]2
SORBIC ACIDINACTIVE INGREDIENTX045WJ989BCLEAN EYES IRRIGANT [WESTWOOD LABORATORIES INC.]2

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 56 of 56 · 1,102 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,Baxter Healthcare Corporatione1953d54-818d-46a6-8532-518ebae6d84e2012-06-13Exact identifier
unii: 451W47IQ8X
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDEBaxter Healthcare Corporationf09f80bf-2f8b-4420-865d-aec2d5e5cd4d2012-06-12Exact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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