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 |
|---|---|---|---|---|---|---|
| Collajoint Lidocaine Pain Relief Gel Patch | LIDOCAINE PAIN RELIEF GEL PATCH | Henan Enokon Medical Instrument Co., Ltd. | 44e27e7f-992f-d194-e063-6294a90a94e4 | 2026-01-31 | Warnings | L7T10EIP3A |
| COLD AND HOT MEDICATED Patch | COLD AND HOT MEDICATED PATCH | Henan Enokon Medical Instrument Co., Ltd. | 49ac6a7b-25d3-6dc4-e063-6394a90a99b6 | 2026-01-31 | Warnings | L7T10EIP3A |
| COLD AND HOT MEDICATED Patch | COLD AND HOT MEDICATED PATCH | Henan Enokon Medical Instrument Co., Ltd. | 49aca763-be2a-cf38-e063-6294a90a092e | 2026-01-31 | Warnings | L7T10EIP3A |
| PAIN RELIEF HOT Patch | PAIN RELIEF HOT PATCH | Henan Enokon Medical Instrument Co., Ltd. | 49ad128a-0f4c-085a-e063-6294a90ac9bb | 2026-01-31 | Warnings | L7T10EIP3A |
| TriDerma Tea Tree Foot Cream | TTM FOOT | Genuine Virgin Aloe Corporation | 49b51d5f-14d1-a5c6-e063-6294a90abdab | 2026-01-31 | Warnings | L7T10EIP3A |
| Optase | GLYCERIN | Scope Health Inc | 376e0289-28e9-e87f-e063-6294a90a3b04 | 2026-01-30 | Warnings | PDC6A3C0OX |
| Walgreens Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Walgreen Company | 3557d2e9-714a-4066-aa73-ea9e3363e574 | 2026-01-30 | Warnings | L7T10EIP3A |
| Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Amazon.com Service LLC | 673996ab-6e57-4feb-8af3-d8b474741a8d | 2026-01-30 | Warnings, Adverse reactions | L7T10EIP3A |
| Anticavity Rinse | SODIUM FLUORIDE | Rite Aid Corporation | c1a22692-b955-498a-a7c1-1cd7bfd54bda | 2026-01-30 | Warnings, Adverse reactions | M021 |
| Oral Sore Antiseptic | HYDROGEN PEROXIDE, MENTHOL | Rite Aid Corporation | e67046ce-bfe0-4454-bbe8-6a3783afb6f5 | 2026-01-30 | Warnings, Adverse reactions | L7T10EIP3A |
| Antiseptic Mouth Rinse | EUCALYPTOL | Rite Aid Corporation | 0f41f4fa-bfcc-4ae7-b173-52a0a9a6366c | 2026-01-30 | Warnings, Adverse reactions | L7T10EIP3A |
| Oral Care Antiseptic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Rite Aid Corporation | c15b31be-a662-4c22-b4a7-66baed20868a | 2026-01-30 | Warnings, Adverse reactions | L7T10EIP3A |
| Antispetic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Rite Aid Corporation | d55d4101-be0c-47d9-a2ad-d3d30516bf04 | 2026-01-30 | Warnings, Adverse reactions | L7T10EIP3A |
| Tartar control plus | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Rite Aid Corporation | a21eef4f-62a5-4f40-8a52-dd581577f7f9 | 2026-01-30 | Warnings, Adverse reactions | L7T10EIP3A |
| Optase | GLYCERIN | Scope Health Inc | 10c3e31d-779d-8ff6-e063-6294a90acd39 | 2026-01-30 | Warnings | PDC6A3C0OX |
| Optase | GLYCERIN | Scope Health Inc | 9e96976b-2990-79e0-e053-2995a90a0f29 | 2026-01-30 | Warnings | PDC6A3C0OX |
| Optase | GLYCERIN | Scope Health Inc | d81c1a4f-87b0-ee8c-e053-2995a90af9e5 | 2026-01-30 | Warnings | PDC6A3C0OX |
| Optase | GLYCERIN | Scope Health Inc | f452a2c4-c869-7bf5-e053-2995a90ac1a0 | 2026-01-30 | Warnings | PDC6A3C0OX |
| Ultra Strength Antacid Assorted Berries | CALCIUM CARBONATE | WAL-MART STORES INC. | 7cfcbb36-c84c-4dc4-873a-ae1c5204aa00 | 2026-01-30 | Warnings | H0G9379FGK |
| ARU GUM HEALTH | STANNOUS FLUORIDE | Ashtel Studios, Inc. | d8e8b92e-d8cb-45ad-8353-7dbe43c3dcd3 | 2026-01-30 | Warnings | M021 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.