Lab52 Anti-Cavity Oral Care

Product NDC: 82711-001
11-digit product format: 827110001
Labeler code: 82711
Product ID: 82711-001_de270f7b-2b8b-8d9e-e053-2995a90a8815
Type: HUMAN OTC DRUG
Nonproprietary name: XYLITOL, CALCIUM LACTATE
Dosage form: AEROSOL
Route: DENTAL
Labeler: TOOTHFILM INC
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2022-05-04
Marketing end: 0000-00-00
Substance: CALCIUM LACTATE; XYLITOL
Active strength: 0 g/100g; g/100g
Pharmacologic classes: Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
82711-001-01	2023-09-26	C162847	48780-1	0191ceaa-66c8-198a-e063-dbdaa90aec3e	de270f7b-2b8a-8d9e-e053-2995a90a8815
82711-001-01	2023-07-28	C162847	48780-1	0191ceaa-66c8-198a-e063-dbdaa90aec3e	de270f7b-2b8a-8d9e-e053-2995a90a8815

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
2URQ2N32W3	CALCIUM LACTATE	814-80-2	CALCIUM LACTATE
VCQ006KQ1E	XYLITOL	87-99-0	XYLITOL

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
82711-001-01	82711000101	20 g in 1 BOTTLE, SPRAY (82711-001-01)	20 g	2022-05-06	0000-00-00	No	No	Current