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Prescription medicine

Anticoagulant citrate phosphate dextrose solution

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

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Quick answers

What is Anticoagulant citrate phosphate dextrose solution used for?
The FDA-approved label (Sterile Cord Blood Collection Unit (Msc123d), Maco Productions, December 16, 2025) says: “MSC123D - For collection of up to 210 mL of umbilical cord blood. Use aseptic technique.” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Anticoagulant citrate phosphate dextrose solution have a boxed warning?
No. None of the 3 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Anticoagulant citrate phosphate dextrose solution?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Anticoagulant citrate phosphate dextrose solution been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Anticoagulant citrate phosphate dextrose solution?
1 company lists prescription products of Anticoagulant citrate phosphate dextrose solution in the FDA NDC Directory, including Maco Productions.

What Anticoagulant citrate phosphate dextrose solution is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

MSC123D - For collection of up to 210 mL of umbilical cord blood. Use aseptic technique.

— FDA label: Sterile Cord Blood Collection Unit (Msc123d), Maco Productions, effective December 16, 2025. Read the full label on DailyMed →

The FDA has 3 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

The label quoted above has no boxed warning.

0 of 3 FDA labels for this medicine have a boxed warning.

Forms and how it is given

Dosage formsInjection, solution
RouteIntravenous
Prescription products3 in the FDA NDC Directory
Brand namesSterile Cord Blood Collection Unit (Msc123d), Sterile Cord Blood Collection Unit (Msc128d), Sterile Cord Blood Collection Unit (Msc127d)

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

No Drugs@FDA application is linked to these products.

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

SPL set ID of the quoted labele3b456ec-4578-485f-a696-8a343505f30b
FDA labels (SPL)3
Active ingredients (FDA)CITRIC ACID MONOHYDRATE / DEXTROSE MONOHYDRATE / SODIUM CITRATE / SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Sterile Cord Blood Collection Unit (Msc123d), Maco Productions, effective December 16, 2025; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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