# CHLORAPREP

NDC: 51662-1675
Generic name: CHLORAPREP
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: TOPICAL
Marketing started: 20240513

FDA application: NDA021555

## Active ingredients

- CHLORHEXIDINE GLUCONATE: 20 mg/mL
- ISOPROPYL ALCOHOL: .7 mL/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1675"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1675
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=44fe08e0-4e9c-8bd6-e063-6394a90a0e2b