NDC 51662-1675 – Chloraprep

Isopropyl Alcohol .7 mL/mL; Chlorhexidine Gluconate 20 mg/mL · Solution · Topical

Human Otc Drug

Product NDC51662-1675

Product details

Brand name
Chloraprep
Generic name
Chloraprep
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
Solution
Route
Topical
Marketing category
NDA · NDA021555
Marketed since
May 13, 2024
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Chloraprep →

Package NDC codes (1)

Package NDCDescriptionSince
51662-1675-11 APPLICATOR in 1 POUCH (51662-1675-1) / 1.75 mL in 1 APPLICATORMay 13, 2024