NDC 0126-0016
PreviDent5000 Dry Mouth 6.1 mg per 1 mL gel, dentifrice
On the label: Colgate Oral Pharmaceuticals, Inc..
Where it's 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 Colgate Oral Pharmaceuticals, Inc. names for other drugs.
Recalls
- Feb 13, 2017 · Class III · Colgate Palmolive Co
Label Mix up; rear panel is incorrectly labeled with the PreviDent 5000 Enamel Protect rear panel.
Lots: Lots: 6350US561G, 6350US562G, 6351US561G, 6351US562G
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fluoride Ion: every company that makes it
- Form
- gel, dentifrice, dental
- Strength
- 6.1 mg per 1 mL
- Approval
- UNAPPROVED DRUG OTHER
- On the market since
- Jul 6, 2009
- Package NDCs
0126-0016-61- Official label
- DailyMed (National Library of Medicine), updated Jun 10, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?