white glo instant white
Generic: sodium monofluorophosphate
Labeler: white glo usa incDrug Facts
Product Profile
Brand Name
white glo instant white
Generic Name
sodium monofluorophosphate
Labeler
white glo usa inc
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
73656-015
Product ID
73656-015_2f18f4c3-ad08-cabf-e063-6294a90a84a3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2021-11-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73656015
Hyphenated Format
73656-015
Supplemental Identifiers
RxCUI
UPC
Packaging Origin
Original Packager
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
white glo instant white (source: ndc)
Generic Name
sodium monofluorophosphate (source: ndc)
Application Number
M021 (source: ndc)
Resolved Composition
Strengths
- 0.1 %
Packaging
- 1 KIT in 1 KIT (73656-015-00) * 1 TUBE in 1 CARTON (73656-016-00) / 150 g in 1 TUBE
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "2f18f4c3-ad08-cabf-e063-6294a90a84a3", "openfda": {"upc": ["0879226001159"], "rxcui": ["545626"], "spl_set_id": ["ce4f0f8f-46f0-b4e6-e053-2a95a90af6c6"], "manufacturer_name": ["WHITE GLO USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (73656-015-00) * 1 TUBE in 1 CARTON (73656-016-00) / 150 g in 1 TUBE", "package_ndc": "73656-015-00", "marketing_start_date": "20211101"}], "brand_name": "White Glo Instant White", "product_id": "73656-015_2f18f4c3-ad08-cabf-e063-6294a90a84a3", "dosage_form": "KIT", "product_ndc": "73656-015", "generic_name": "SODIUM MONOFLUOROPHOSPHATE", "labeler_name": "WHITE GLO USA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "White Glo Instant White", "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211101", "listing_expiration_date": "20261231"}