Periogard

ANDA 73695, held by Colgate Palmolive Co. Chlorhexidine Gluconate.

As of Nov 15, 2026, ANDA 73695 (Periogard), held by Colgate Palmolive Co, was first approved by FDA on Jan 14, 1994, with 13 approved supplements and 0 published complete response letters.

First approved: Jan 14, 1994
Supplements approved: 13
Complete response letters: 0

Approvals and New Uses

The original application and every efficacy supplement, newest first; all 14 submissions below

Date	Submission	Status	Documents
Jan 14, 1994	Original application	Approved	Review

Products

1 strengths and forms

Product	Active ingredient	Marketing
Periogard0.12% · solution;dental	Chlorhexidine Gluconate	Discontinued

All 14 submissions, including labeling and manufacturing supplements


Jan 14, 2009	Supplement 20Labeling	Approved	None posted
Nov 15, 1999	Supplement 13Manufacturing	Approved	None posted
Nov 15, 1999	Supplement 14Labeling	Approved	None posted
Jul 1, 1999	Supplement 15Manufacturing	Approved	None posted
Oct 29, 1998	Supplement 12Manufacturing	Approved	None posted
Dec 11, 1997	Supplement 11Labeling	Approved	None posted
Jul 8, 1997	Supplement 10Manufacturing	Approved	None posted
Apr 7, 1997	Supplement 7Manufacturing	Approved	None posted
Apr 7, 1997	Supplement 8Manufacturing	Approved	None posted
Dec 13, 1996	Supplement 6Manufacturing	Approved	None posted
May 1, 1996	Supplement 5Manufacturing	Approved	None posted
Feb 12, 1996	Supplement 4Labeling	Approved	None posted
Jun 16, 1994	Supplement 1Manufacturing	Approved	None posted
Jan 14, 1994	Original application	Approved	Review

Identifiers

Application: ANDA 73695
Drugs@FDA: Overview at FDA
Company: Colgate-Palmolive

Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters