NDC 21695-025
Chlorhexidine Gluconate 0.12 mg per 1 mL rinse
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Xttrium Laboratories, Inc.'s NDC 0116-2001.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Xttrium Laboratories, Inc. | Mount Prospect, IL, United States | Makes it | Problems found, fixed voluntarilyJun 16, 2026 · 17 inspections, 2 with FDA action |
Recalls
- Jun 1, 2017 · Class II · Xttrium Laboratories Inc
CGMP Deviations
Lots: 1999CHG16MC-Lot number 704-201 (full lot # 704-1999-201), Exp 03/20 1999CHG16MC-Lot number 705-208 (full lot # 705-1999-208), Exp 04/20
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Chlorhexidine: every company that makes it
- Form
- rinse
- Strength
- 0.12 mg per 1 mL
- Approval
- ANDA ANDA077789
- On the market since
- Aug 1, 2009
- Package NDCs
21695-025-16- Official label
- DailyMed (National Library of Medicine), updated Sep 23, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?