optimax purple anticavity fluoride

Generic: sodium monofluorophosphate

Labeler: white glo usa inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name optimax purple anticavity fluoride
Generic Name sodium monofluorophosphate
Labeler white glo usa inc
Dosage Form KIT
Manufacturer
WHITE GLO USA INC

Identifiers & Regulatory

Product NDC 73656-039
Product ID 73656-039_40307605-5786-4ddd-e063-6294a90a1f64
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2025-12-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73656039
Hyphenated Format 73656-039

Supplemental Identifiers

RxCUI
545626
UPC
0879226001906

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name optimax purple anticavity fluoride (source: ndc)
Generic Name sodium monofluorophosphate (source: ndc)
Application Number M021 (source: ndc)

Resolved Composition

Strengths
  • 0.76 %
  • 0.1 %
source: label
Packaging
  • 1 KIT in 1 KIT (73656-039-00) * 1 TUBE in 1 BOX (73656-040-00) / 150 g in 1 TUBE
source: ndc

Packages (1)

73656-039-00 1 KIT in 1 KIT (73656-039-00) * 1 TUBE in 1 BOX (73656-040-00) / 150 g in 1 TUBE

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Optimax Purple Anticavity Fluoride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "40307605-5786-4ddd-e063-6294a90a1f64", "openfda": {"upc": ["0879226001906"], "rxcui": ["545626"], "spl_set_id": ["fdb16e59-5be1-4bd0-a940-d542d67fb2df"], "manufacturer_name": ["WHITE GLO USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (73656-039-00)  *  1 TUBE in 1 BOX (73656-040-00)  / 150 g in 1 TUBE", "package_ndc": "73656-039-00", "marketing_start_date": "20251208"}], "brand_name": "Optimax Purple Anticavity Fluoride", "product_id": "73656-039_40307605-5786-4ddd-e063-6294a90a1f64", "dosage_form": "KIT", "product_ndc": "73656-039", "generic_name": "SODIUM MONOFLUOROPHOSPHATE", "labeler_name": "WHITE GLO USA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Optimax Purple Anticavity Fluoride", "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251208", "listing_expiration_date": "20261231"}