Chloraprep 51662-1675
Product NDC
51662-1675- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Solution
- Route
- Topical
- Product Type
- Human Otc Drug
- Marketing Start
- May 13, 2024
- Listing Expires
- December 31, 2026
- Application
- NDA021555
Active Ingredients
| Ingredient | Strength |
|---|---|
| Chlorhexidine Gluconate | 20 mg/mL |
| Isopropyl Alcohol | .7 mL/mL |
Drug Class
Decreased Cell Wall Integrity [PE]
Packaging Options(1)
1 APPLICATOR in 1 POUCH (51662-1675-1) / 1.75 mL in 1 APPLICATOR