optimax anticavity fluoride watermelon

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 anticavity fluoride watermelon
Generic Name sodium monofluorophosphate
Labeler white glo usa inc
Dosage Form PASTE
Routes
DENTAL
Active Ingredients

sodium monofluorophosphate 7.6 mg/g

Manufacturer
WHITE GLO USA INC

Identifiers & Regulatory

Product NDC 73656-032
Product ID 73656-032_34f34256-f481-6fe6-e063-6394a90af80b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2025-04-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73656032
Hyphenated Format 73656-032

Supplemental Identifiers

RxCUI
545626
UNII
C810JCZ56Q

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 anticavity fluoride watermelon (source: ndc)
Generic Name sodium monofluorophosphate (source: ndc)
Application Number M021 (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 7.6 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 BOX (73656-032-00) / 80 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (1)

sodium monofluorophosphate (7.6 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "34f34256-f481-6fe6-e063-6394a90af80b", "openfda": {"unii": ["C810JCZ56Q"], "rxcui": ["545626"], "spl_set_id": ["b506df13-649f-4615-bc25-6ae08bd56b18"], "manufacturer_name": ["WHITE GLO USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (73656-032-00)  / 80 g in 1 TUBE", "package_ndc": "73656-032-00", "marketing_start_date": "20250404"}], "brand_name": "Optimax Anticavity Fluoride Watermelon", "product_id": "73656-032_34f34256-f481-6fe6-e063-6394a90af80b", "dosage_form": "PASTE", "product_ndc": "73656-032", "generic_name": "SODIUM MONOFLUOROPHOSPHATE", "labeler_name": "WHITE GLO USA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Optimax Anticavity Fluoride Watermelon", "active_ingredients": [{"name": "SODIUM MONOFLUOROPHOSPHATE", "strength": "7.6 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250404", "listing_expiration_date": "20261231"}