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 69 of 223 · 4,451 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Botao Kids Strawberry Flavored with Fluoride BOTAO KIDS STRAWBERRY FLAVORED TOOTHPASTE WITH FLUORIDE Peer Pharm Ltd. 48b8d884-5e15-4145-8521-ae9ee482e392 2026-01-12 Warnings Exact identifier application number: M021 LONAZEM MENTHOL,PETROLATUM PEER PHARM LTD. 91f7a741-4178-4639-9cd5-746a4b9a21bf 2026-01-12 Warnings Exact identifier unii: L7T10EIP3A Mineral Ice Pain Relieving MENTHOL Crown Laboratories 7b30076a-0af6-2f74-e053-2a91aa0ae08d 2026-01-12 Warnings Exact identifier unii: L7T10EIP3A Sarna PRAMOXINE HYDROCHLORIDE, MENTHOL Crown Laboratories, Inc 19c41e75-a654-90cf-e063-6394a90a7e97 2026-01-12 Warnings Exact identifier unii: L7T10EIP3A BlueStop Max EXTERNAL ANALGESIC Clavel Corporation f1efb51c-5217-4cb2-e053-2a95a90a7f95 2026-01-12 Warnings Exact identifier unii: L7T10EIP3A Extra Strength Balm CAPSICUM AND MENTHOL Saje Natural Business Inc f516e416-446b-8f21-e053-2a95a90afd88 2026-01-12 Warnings Exact identifier unii: L7T10EIP3A Pain Release MENTHOL Saje Natural Business Inc. 3df0e56a-7651-42dc-8ed8-f68836a63c61 2026-01-12 Warnings Exact identifier unii: L7T10EIP3A Trauma Less MENTHOL Saje Natural Business Inc. 650cba4c-6aba-48c3-9c41-841f19905548 2026-01-12 Warnings Exact identifier unii: L7T10EIP3A Chest Comfort MENTHOL Saje Natural Business Inc. 8a3db169-6dd7-4dfd-8360-90315288f21b 2026-01-12 Warnings Exact identifier unii: L7T10EIP3A ACT Total Care Anticavity Fluoride Fresh Mint SODIUM FLUORIDE Chattem, Inc. 4ee6a478-afcf-4540-b427-ba08c942ccb3 2026-01-12 Warnings Exact identifier application number: M021 ACT Anticavity Fluoride Mint SODIUM FLUORIDE Chattem, Inc. e81c83a2-363a-442f-8731-2598a4f4c21e 2026-01-12 Warnings Exact identifier application number: M021 CVS Health Extra Strength Sugar Free Antacid ANTACID CVS Pharmacy,Inc. f722e7ce-6cca-4850-a230-7510c7ca7754 2026-01-12 Warnings Exact identifier unii: H0G9379FGK ACT Total Care Anticavity Fluoride Icy Clean Mint SODIUM FLUORIDE Chattem, Inc. 258b78b4-55e7-410c-90f8-a3e456c02579 2026-01-12 Warnings Exact identifier application number: M021 ACT Total Care Dry Mouth Anticavity Mouth SODIUM FLUORIDE Chattem, Inc. 06684b82-aaa0-4ca6-8d56-4f9866269000 2026-01-12 Warnings Exact identifier application number: M021 ACT Anticavity Fluoride Kids Groovy Grape SODIUM FLUORIDE Chattem, Inc. cd167c0b-2086-4204-b0ac-90df404bd4bb 2026-01-12 Warnings Exact identifier application number: M021 ACT Total Care Anticavity Fluoride Icy Clean Mint SODIUM FLUORIDE Chattem, Inc. beded786-bb55-4ba3-82fe-9e9d1b5e2979 2026-01-12 Warnings Exact identifier application number: M021 ACT Kids Pure Protect Anticavity- Simply Strawberry SODIUM FLUORIDE Chattem, Inc. 2fc80727-57c7-4a33-80e0-ab9f9487390d 2026-01-12 Warnings Exact identifier application number: M021 ACT Kids Anticavity Fluoride Groovy Grape SODIUM FLUORIDE Chattem, Inc. 310a3c11-1c66-4dac-99f4-5fdc15d0f77c 2026-01-12 Warnings Exact identifier application number: M021 ACT Anticavity Fluoride Kids Bubblegum SODIUM FLUORIDE Chattem, Inc. fbbccd58-a816-4a93-a658-f28246c11e80 2026-01-12 Warnings Exact identifier application number: M021 ACT Whitening Anticavity Gentle Mint SODIUM FLUORIDE 0.02 (0.009 W/V FLUORIDE ION) Chattem, Inc. cd45a0b8-9ab3-4aed-8214-a6dcc4cdaf49 2026-01-12 Warnings Exact identifier application number: M021
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.