NDC 70166-027
Chlorhexidine Gluconate 1.2 mg per 1 mL rinse
On the label: Lohxa. It's repackaged from NDC 52376-021, made by Sunstar Americas, Inc. (Paroex). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Lohxa names for other drugs.
Recalls
- Oct 28, 2020 · Class I · Lohxa LLC
Microbial contamination of non-sterile products: Repackaged product was recalled by manufacturer because it was contaminated with the bacteria Burkholderia lata.
Lots: Lot #: T09101A, Exp 01/2021; T08292A, T10011A, Exp 02/2021; T10223A, M10193A, Exp 03/2021
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
- 1.2 mg per 1 mL
- Approval
- ANDA ANDA076434
- On the market since
- Aug 23, 2019
- Package NDCs
70166-027-15- Official label
- DailyMed (National Library of Medicine), updated Feb 25, 2021
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