Home NDC 73656-035 NDC 73656-035 - Optimax Purple Anticavity Fluoride This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 73656-035
Package NDCs from labels 73656-035-00
Manufacturer WHITE GLO USA INC
Effective date 2025-09-02
Current FDA listing Not matched in FDA.report NDC product tables openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 116 of 223 · 4,451 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pepcid Complete FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE Kenvue Brands LLC 37e6a3f6-5261-475d-a7d4-e72854088982 2025-11-05 Warnings Exact identifier unii: H0G9379FGK Good Neighbor Pharmacy Medicated Chest Rub CAMPHOR, MENTHOL, EUCALYPTUS OIL AMERISOURCE BERGEN c1843f1a-ae5b-0fdf-e053-2995a90aae38 2025-11-05 Warnings Exact identifier unii: L7T10EIP3A Pranicura 5 GLYCERIN, KAOLIN, CALAMINE, MENTHOL Pranicura Products LLC af520a58-3f3c-4d28-a41f-3ed8f74da095 2025-11-04 Warnings Exact identifier unii: PDC6A3C0OX unii: L7T10EIP3A WALGREENS EXTRA STRENGTH SMOOTH ANTACID CALCIUM CARBONATE WALGREENS CO. 9a5631e8-4287-4368-bb56-3ce22a3680d8 2025-11-04 Warnings Exact identifier unii: H0G9379FGK up and up extra strength antacid 750 Assorted Berry ANTACID TABLETS Target Corporation 46f11acf-a968-4fdd-8755-3eff0b9b67d0 2025-11-04 Warnings Exact identifier unii: H0G9379FGK up and up extra strength antacid 750 Assorted Berry ANTACID TABLETS Target Corporation b76441ad-f701-4d0d-b9a7-18ac466faa44 2025-11-04 Warnings Exact identifier unii: H0G9379FGK extra strength Tropical Fruit ANTACID Target Corporation b2c2fcb4-5a47-47eb-ae0e-6bc3713b161d 2025-11-04 Warnings Exact identifier unii: H0G9379FGK ultra strength Assorted Fruit CALCIUM CARBONATE ANTACID Target Corporation a0f2ac91-c425-4e6d-8dd6-224a5b85cd2e 2025-11-04 Warnings Exact identifier unii: H0G9379FGK ultra strength antacid Peppermint Flavored CALCIIUM CARBONATE Target Corporation 55dc1614-8fc0-4f2c-abfc-b675173b4f07 2025-11-04 Warnings Exact identifier unii: H0G9379FGK ultra strength antacid ANTACID Target Corporation 2125e81b-23c6-4c5f-a6aa-829f8d3df71f 2025-11-04 Warnings Exact identifier unii: H0G9379FGK up and up extra strength smooth dissolving antacid Assorted berry ANTACID TABLETS Target Corporation e78afe7b-a835-4fdb-9ef8-0499d1a83e6e 2025-11-04 Warnings Exact identifier unii: H0G9379FGK up and up extra strength smooth dissolving antacid Assorted Fruit CALCIUM CARBONATE Target corporation b97558c5-d836-42ae-bfa5-0f4c6bca7e4a 2025-11-04 Warnings Exact identifier unii: H0G9379FGK Ultra Strength Antacid CALCIUM CARBONATE PEPPERMINT TARGET CORPORATION 07aa98b3-699a-bf8d-e063-6294a90a2dee 2025-11-04 Warnings Exact identifier unii: H0G9379FGK Extra Strength Antacid Calcium Carbonate,750 mg CALCIUM CARBONATE TARGET CORPORATION 07aa39bb-c409-ce4f-e063-6394a90a7069 2025-11-04 Warnings Exact identifier unii: H0G9379FGK Bacteriostatic Water BACTERIOSTATIC WATER ProPharma Distribution 42c6938e-f747-ae13-e063-6294a90a59a3 2025-11-04 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R Pain Relief Gel-Roll On LIDOCAINE AND MENTHOL Bullet point LLC 42c70681-494b-47c9-e063-6394a90a80be 2025-11-04 Warnings Exact identifier unii: L7T10EIP3A Dentisse SODIUM FLUORIDE Dentisse, Inc. 326b290a-9bd2-468e-e054-00144ff8d46c 2025-11-04 Warnings Exact identifier application number: M021 Home Care Fluoride STANNOUS FLUORIDE Dental Technologies, Inc. 51f1d84c-809a-4c96-a117-7a8d8aa1e6b4 2025-11-04 Warnings Exact identifier application number: M021 Home Care Fluoride STANNOUS FLUORIDE Dental Technologies, Inc. c44686f8-93ee-4a8f-8481-3439d123f6d2 2025-11-04 Warnings Exact identifier application number: M021 Home Care Fluoride STANNOUS FLUORIDE Dental Technologies, Inc. 16ebcb37-5703-4e10-b965-570e18434b52 2025-11-04 Warnings Exact identifier application number: M021
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.