ACD-A

Manufacturer
Fenwal, Inc. | Fenwal International, Inc.
Effective date
2022-11-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
9
Source
legacy-cache
Hydrated at
2026-08-01 21:50:04

Label at a glance#

ProductACD-A
Active ingredientDEXTROSE MONOHYDRATE, SODIUM CITRATE, UNSPECIFIED FORM, ANHYDROUS CITRIC ACID
Label structure3 sections

Label contents#

Full prescribing information#

WARNINGS

WARNINGS SECTION

Do Not Use Unless Solution is Clear and Seal is Intact

HOW SUPPLIED

HOW SUPPLIED SECTION

Sterile, Non-pyrogenic

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hotstamp
Hotstamp

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0942-9005ACD-A (ANTIOCOAGULANT CITRATE DEXTROSE SOLUTION, FORMULA A) SOLUTION [FENWAL, INC.]9Legacy NDC20221102_bee8e967-496c-4541-b092-ead6c8c80269.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANHYDROUS CITRIC ACIDACTIVE INGREDIENTXF417D3PSL7
DEXTROSE MONOHYDRATEACTIVE INGREDIENTLX22YL083G7
SODIUM CITRATEACTIVE INGREDIENT1Q73Q2JULR7
ANHYDROUS CITRIC ACIDACTIVE MOIETYXF417D3PSL7
ANHYDROUS DEXTROSEACTIVE MOIETY5SL0G7R0OK7

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0942-90050942-9005-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
dec66999-e30e-406b-aeb2-7df043806861bee8e967-496c-4541-b092-ead6c8c802692025-11-26WarningsExact identifier
spl set id: bee8e967-496c-4541-b092-ead6c8c80269

Reported adverse events (FAERS/openFDA)#

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