Package 73656-039-00

Brand: optimax purple anticavity fluoride

Generic: sodium monofluorophosphate
NDC Package

Package Facts

Identity

Package NDC 73656-039-00
Digits Only 7365603900
Product NDC 73656-039
Product ID 73656-039_40307605-5786-4ddd-e063-6294a90a1f64
Description

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

Marketing

Marketing Status
Marketed Since 2025-12-08
Brand optimax purple anticavity fluoride
Generic sodium monofluorophosphate
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

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"}