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 |
|---|---|---|---|---|---|---|
| Super Mint | SUPER MINT TOOTHPASTE | SuperMouth, LLC. | be0915f3-36c4-4200-9d15-704cfbd632b4 | 2025-07-05 | Warnings | M021 |
| Super Vanilla | VANILLA TOOTHPASTE | SuperMouth, LLC. | 3ddfe20a-86f1-4566-bb77-82c9749411f6 | 2025-07-05 | Warnings | M021 |
| Super Chocolate | CHOCOLATE TOOTHPASTE | SuperMouth, LLC. | 48607622-7c5e-4ddc-8d83-707f26c0553f | 2025-07-05 | Warnings | M021 |
| Stopain Extra Strength | MENTHOL | Troy Manufacturing, Inc. | 07e9a235-6d10-4407-8729-beaf936e97ad | 2025-07-03 | Warnings | L7T10EIP3A |
| Blue Ice Topical Analgesic Gel | ICE GEL | International Wholesale | 397cd306-078d-5b7d-e063-6294a90a8bbc | 2025-07-03 | Warnings | L7T10EIP3A |
| Hemorrhoidal Cream | GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM | Trifecta Pharmaceuticals Usa Llc | 38cf4e43-280b-eb96-e063-6294a90a5949 | 2025-07-02 | Warnings | PDC6A3C0OX |
| 24/7 Life Medicated Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL OINTMENT | Lil' Drug Store Products, Inc. | f03430d4-8dbb-4fc0-e053-2a95a90a119d | 2025-07-02 | Warnings | L7T10EIP3A |
| LIDOCAINE | LIDOCAINE, MENTHOL | Vive Health LLC | 236ccc6d-21b7-6153-e063-6394a90a4634 | 2025-07-02 | Warnings | L7T10EIP3A |
| AsperFlex MAX | LIDOCAINE 4% WITH MENTHOL 1% | Akron Pharma Inc. | ccf6172b-350a-4b78-b844-f84bf17c491f | 2025-07-02 | Warnings | L7T10EIP3A |
| topcare dual action complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Topco Associates LLC | 8ef70327-9a04-413b-b331-f5d3a94d6b36 | 2025-07-01 | Warnings | H0G9379FGK |
| SEFUDUN FUNGAL NAIL PATCHES | GLYCERIN | Shenzhen Shandian Jingling Technology Co., Ltd. | 38db97d6-27c8-da99-e063-6294a90aac66 | 2025-07-01 | Warnings | PDC6A3C0OX |
| KOSHER MEDS antacid | CALCIUM CARBONATE | Mollec Inc | 7783d6a2-56e3-4542-ad1d-60680e03532b | 2025-07-01 | Warnings | H0G9379FGK |
| Acid Reducer Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Walgreen Company | 3a456dab-0a2d-4e48-a8e2-e49a7acef963 | 2025-07-01 | Warnings | H0G9379FGK |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | H E B | c1aa7efa-4be1-4c8f-8994-661dd60e1aa9 | 2025-07-01 | Warnings | H0G9379FGK |
| leader acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Cardinal Health 110, LLC. dba Leader | a5420ef1-313f-4561-baf1-7ae017ea343a | 2025-07-01 | Warnings | H0G9379FGK |
| Bonica EaseX Pain Relieving | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE | Planet (Anhui) Pharmaceutical Co., Ltd. | 34f1196a-fda1-4bef-be71-e5a09ee97bc1 | 2025-06-27 | Warnings | L7T10EIP3A |
| Medline | MENTHOL | Medline Industries, LP | 0d947aa6-045e-d001-e063-6294a90a3657 | 2025-06-26 | Warnings | L7T10EIP3A |
| Sugar Free Cough Drops | MENTHOL | CVS Pharmacy | f038b713-0721-2bb5-e053-2a95a90a7842 | 2025-06-26 | Warnings | L7T10EIP3A |
| PHIZICO Pain Relief | MENTHOL | ER3 BRANDS INC. | 72715dc5-d1e7-4b4b-8e28-4e367abba322 | 2025-06-25 | Warnings | L7T10EIP3A |
| Diva Cramp Care Cream | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | 37368566-b14e-4d5c-bdde-6eea9073974f | 2025-06-25 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.