FDA.reportPublic FDA data

NDC11 52268010001

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDCProduct root
52268-0100-0152268-0100
52268-0100-152268-0100
52268-100-0152268-100

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GoLYTELYPOLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDEBraintree Laboratories, Inc.57d22b0b-1ae0-4203-babc-f3bac17bd1c92021-05-28Warnings, Adverse reactionsExact identifier
ndc (package): 52268-100-01
ndc (product): 52268-100
ndc11 (package): 52268010001