61578-215Level 3
PRO Gel 5000 (Sodium fluoride)
**Product type:** Human Prescription Drug
**Active ingredient:** SODIUM FLUORIDE
**Strength:** 5000 ug/g
**Dosage form:** Gel, Dentifrice
**Route:** Dental
**Labeler:** DENTAL ALLIANCE HOLDINGS LLC
**Marketing category:** UNAPPROVED DRUG OTHER
GET
/api/v1/systems/ndc_fda/nodes/61578-215Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.