Chloraprep NDC 51662-1675

NDC codes

FDA NDC Directory

Product NDC (as listed)51662-1675Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51662-1675Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
51662-1675-1	51662167501	1 APPLICATOR in 1 POUCH (51662-1675-1) / 1.75 mL in 1 APPLICATORMarketed from May 13, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Chloraprep
Generic name (nonproprietary): chloraprep
Active ingredients: Isopropyl alcohol — .7 mL/mLChlorhexidine gluconate — 20 mg/mL
Dosage form: Solution
Route: Topical
Labeler: HF Acquisition Co LLC, DBA HealthFirst
Product type: Over-the-counter drug
Marketing category: NDA — New Drug ApplicationApplication NDA 021555
Marketing start: May 13, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Cell Wall Integrity (Physiologic effect)
Identifiers: Product ID 51662-1675_44fe08e0-4e9d-8bd6-e063-6394a90a0e2bSPL ID 44fe08e0-4e9d-8bd6-e063-6394a90a0e2bSPL set ID 44fe08e0-4e9c-8bd6-e063-6394a90a0e2bUNII ND2M416302, MOR84MUD8E

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N451662167501 followed by a unit qualifier and the quantity

Package 51662-1675-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 2, 2025.

Indications (excerpt from the label)

for the preparation of the patient's skin prior to surgery. Helps to reduce bacteria that potentially can cause skin infection.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 021555

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 021555
Product	Strength	Form · route	Labeler	Product NDC
ChloraPrep One-Stepchlorhexidine gluconate and isopropyl alcohol	Chlorhexidine gluconate 20 mg/mL; Isopropyl alcohol .7 mL/mL	SolutionTopical	CareFusion 213 LLC	54365-400
ChloraPrep Swabstickchlorhexidine gluconate and isopropyl alcohol	Chlorhexidine gluconate 20 mg/mL; Isopropyl alcohol .7 mL/mL	SolutionTopical	CareFusion 213 LLC	54365-401