white glo bio-enzyme

Generic: sodium monofluorophosphate

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

Drug Facts

Product Profile

Brand Name white glo bio-enzyme
Generic Name sodium monofluorophosphate
Labeler white glo usa inc
Dosage Form KIT
Manufacturer
WHITE GLO USA INC

Identifiers & Regulatory

Product NDC 73656-005
Product ID 73656-005_2f18bf4f-05b2-3f57-e063-6394a90aa4aa
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2020-02-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73656005
Hyphenated Format 73656-005

Supplemental Identifiers

RxCUI
545626
UPC
0879226001012

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 white glo bio-enzyme (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 (73656-005-00) * 150 g in 1 TUBE (73656-006-00)
source: ndc

Packages (1)

73656-005-00 1 KIT in 1 KIT (73656-005-00) * 150 g in 1 TUBE (73656-006-00)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

WHITE GLO BIO-ENZYME ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "2f18bf4f-05b2-3f57-e063-6394a90aa4aa", "openfda": {"upc": ["0879226001012"], "rxcui": ["545626"], "spl_set_id": ["f894a841-0df7-470d-8fc2-c9d6ba0edf99"], "manufacturer_name": ["WHITE GLO USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (73656-005-00)  *  150 g in 1 TUBE (73656-006-00)", "package_ndc": "73656-005-00", "marketing_start_date": "20200215"}], "brand_name": "WHITE GLO BIO-ENZYME", "product_id": "73656-005_2f18bf4f-05b2-3f57-e063-6394a90aa4aa", "dosage_form": "KIT", "product_ndc": "73656-005", "generic_name": "SODIUM MONOFLUOROPHOSPHATE", "labeler_name": "WHITE GLO USA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "WHITE GLO BIO-ENZYME", "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200215", "listing_expiration_date": "20261231"}