Package 73656-036-00

Brand: optimax professional whitening anticavity fluoride

Generic: sodium monofluorophosphate
NDC Package

Package Facts

Identity

Package NDC 73656-036-00
Digits Only 7365603600
Product NDC 73656-036
Product ID 73656-036_3f1861dc-cfda-39f6-e063-6294a90ac367
Description

1 KIT in 1 KIT (73656-036-00) * 1 TUBE in 1 BOX (73656-037-00) / 150 g in 1 TUBE

Marketing

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

Linked Drug Pages (1)

Optimax Professional Whitening Anticavity Fluoride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "3f1861dc-cfda-39f6-e063-6294a90ac367", "openfda": {"upc": ["0879226001883"], "rxcui": ["545626"], "spl_set_id": ["8c4b9db9-8f23-4dd5-ab6e-1c2f9a3da5b1"], "manufacturer_name": ["WHITE GLO USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (73656-036-00)  *  1 TUBE in 1 BOX (73656-037-00)  / 150 g in 1 TUBE", "package_ndc": "73656-036-00", "marketing_start_date": "20251208"}], "brand_name": "Optimax Professional Whitening Anticavity Fluoride", "product_id": "73656-036_3f1861dc-cfda-39f6-e063-6294a90ac367", "dosage_form": "KIT", "product_ndc": "73656-036", "generic_name": "SODIUM MONOFLUOROPHOSPHATE", "labeler_name": "WHITE GLO USA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Optimax Professional Whitening Anticavity Fluoride", "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251208", "listing_expiration_date": "20261231"}