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
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Optimax Purple Anticavity Fluoride - WHITE GLO USA INC | WHITE GLO USA INC | 2025-09-02 | HUMAN OTC DRUG LABEL |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Eagle Brand Medicated Oil | MENTHOL, METHYL SALICYLATE | PT. EAGLE INDO PHARMA | 5071f145-49f7-0855-e063-6394a90a8f26 | 2026-04-27 | Warnings | L7T10EIP3A |
| Eagle Brand Medicated Oil Refresh | CAMPHOR, MENTHOL | PT. EAGLE INDO PHARMA | 09260c31-56a3-07aa-e063-6394a90a95fd | 2026-04-27 | Warnings | L7T10EIP3A |
| Eagle Brand Muscle Rub | MENTHOL, METHYL SALICYLATE | PT. EAGLE INDO PHARMA | 5072ad57-9fa7-ddba-e063-6394a90a319b | 2026-04-27 | Warnings | L7T10EIP3A |
| Alcohol Free Refreshing Mint | SODIUM FLUORIDE | H E B | cedf7c08-7412-4733-9b67-225b331cec8c | 2026-04-27 | Warnings, Adverse reactions | M021 |
| Eagle Brand Medicated Roll On Refresh | CAMPHOR, MENTHOL | PT. EAGLE INDO PHARMA | 09235f26-2262-6ca2-e063-6394a90ad8f1 | 2026-04-27 | Warnings | L7T10EIP3A |
| Eagle Brand Medicated Roll On Aromatic | CAMPHOR, MENTHOL, METHYL SALICYLATE | PT. EAGLE INDO PHARMA | 0f333f93-bec6-72d5-e063-6394a90a4e3f | 2026-04-27 | Warnings | L7T10EIP3A |
| anzoon ANTIBACTERIAL MOUTH WASH | CETYLPYRIDINIUM CHLORIDE | Shandong AZC Biotechnology Co.,Ltd. | 507c6896-2806-790c-e063-6394a90ac5ce | 2026-04-27 | Warnings | M021 |
| REFRESH TEARS PF | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN | Allergan, Inc. | 9e1cba7b-84ed-47f3-b19a-121992834350 | 2026-04-24 | Warnings | PDC6A3C0OX K679OBS311 |
| Mylanta All-Family Multi Symptom Stomach Remedy | CALCIUM CARBONATE, SIMETHICONE | Sportpharm LLC | a70f113d-d5a3-44f5-b223-cd1b0e159e1a | 2026-04-24 | Warnings | H0G9379FGK |
| HIP PAIN RELIEF ROLL-ON | LIDOCAINE AND MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 502f1f9e-8552-ca7b-e063-6394a90a7c53 | 2026-04-24 | Warnings | L7T10EIP3A |
| Pharmacy Choice | MENTHOL, ZINC OXIDE | PHARMACY CHOICE INC | 5031fc05-e1c7-40b1-e063-6394a90aa12c | 2026-04-24 | Warnings | L7T10EIP3A |
| DELTA COMFORT PLUS AMENITY | SODIUM MONOFLUOROPHOSPHATE | Buzz Products Inc. | 26434794-ae02-0f58-e063-6294a90ad85e | 2026-04-24 | Warnings | M021 545626 |
| SOMBRA WARM THERAPY | MENTHOL CAMPHOR | SOMBRA COSMETICS INC. | de78dba9-53b3-4dbd-9dd2-6a692378da34 | 2026-04-24 | Warnings | L7T10EIP3A |
| A and H Plus Therabreath Breath Freshners | SODIUM FLUORIDE | Church & Dwight Co., Inc. | 18d6073e-b1ee-47d2-9758-2cf04f3cf3ca | 2026-04-23 | Warnings | M021 |
| Prenatal Plus Vitamins | PRENATAL WITH FERROUS FUMARATE AND FOLIC ACID | REMEDYREPACK INC. | 1b8ef3ea-5563-48ef-ba5e-27e0b454efb9 | 2026-04-23 | Boxed warning | H0G9379FGK |
| Fluoride | SODIUM FLUORIDE | McKesson | 5025e58e-e59c-07b6-e063-6394a90ac1e8 | 2026-04-23 | Warnings | M021 |
| PRO-SYS | SENSITIVITY - MINT (OTC) | Benco Dental | 4e46847e-8c1d-c988-e063-6394a90a8e50 | 2026-04-22 | Warnings | M021 |
| Anticavity Fluoride Rinse | SODIUM FLUORIDE | H E B | 87327a36-a314-4daa-83b6-b4bd3e26bba2 | 2026-04-22 | Warnings, Adverse reactions | M021 |
| Anticavity | SODIUM FLUORIDE | H E B | 8df324a7-9204-40f3-8ddb-1656286d7d4e | 2026-04-22 | Warnings, Adverse reactions | M021 |
| Colgate Total SF Whitening | STANNOUS FLUORIDE | Colgate-Palmolive Company | 3bba340e-2a62-3b04-41b5-0ed9c13adb13 | 2026-04-22 | Warnings | M021 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.