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FDA Approval

Periogard Alcohol Free

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Effective Date
November 18, 2020
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Chlorhexidine(1.2 mg in 1 mL)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Periogard Alcohol Free

Product Details

NDC Product Code
0126-0272
Application Number
ANDA203212
Marketing Category
ANDA (C73584)
Route of Administration
BUCCAL
Effective Date
November 18, 2020
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3Class: IACT
GLYCERINInactive
Code: PDC6A3C0OXClass: IACT
SORBITOLInactive
Code: 506T60A25RClass: IACT
Code: MOR84MUD8EClass: ACTIBQuantity: 1.2 mg in 1 mL
WATERInactive
Code: 059QF0KO0RClass: IACT
CETYLPYRIDINIUM CHLORIDEInactive
Code: D9OM4SK49PClass: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBDClass: IACT
PEG-40 CASTOR OILInactive
Code: 4ERD2076EFClass: IACT
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