Optimax Professional Whitening Anticavity Fluoride

SPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerWHITE GLO USA INC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7365603800
1 KIT in 1 KIT (73656-038-00) * 1 TUBE in 1 BOX (73656-037-00) / 150 g in 1 TUBE

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": null,
  "spl_meta": {
    "fdb16e59-5be1-4bd0-a940-d542d67fb2df": {
      "match": "brand_token",
      "title": "OPTIMAX PURPLE ANTICAVITY FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) KIT [WHITE GLO USA INC]",
      "spl_version": "1",
      "published_date": "2025-12-15"
    }
  },
  "productid": "73656-038_3f187626-b3c5-6648-e063-6294a90a7836",
  "productndc": "73656-038",
  "dosage_form": "KIT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": null,
  "proprietary_name": "Optimax Professional Whitening Anticavity Fluoride",
  "active_ingred_unit": null,
  "application_number": "M021",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "SODIUM MONOFLUOROPHOSPHATE",
  "start_marketing_date": "20251208",
  "active_numerator_strength": null
}

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