alpha-pro

Generic: sodium fluoride and hydrofluoric acid

Labeler: dental technologies, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name alpha-pro
Generic Name sodium fluoride and hydrofluoric acid
Labeler dental technologies, inc.
Dosage Form GEL
Routes
DENTAL
Active Ingredients

hydrofluoric acid 4.4 mg/g, sodium fluoride 7.9 mg/g

Manufacturer
Dental Technologies, Inc.

Identifiers & Regulatory

Product NDC 55346-0942
Product ID 55346-0942_42c8ae03-7559-51a8-e063-6394a90ab69e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2013-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 553460942
Hyphenated Format 55346-0942

Supplemental Identifiers

RxCUI
1297381
UNII
RGL5YE86CZ 8ZYQ1474W7

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 alpha-pro (source: ndc)
Generic Name sodium fluoride and hydrofluoric acid (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 4.4 mg/g
  • 7.9 mg/g
source: ndc
Packaging
  • 497 g in 1 BOTTLE (55346-0942-1)
source: ndc

Packages (1)

Ingredients (2)

hydrofluoric acid (4.4 mg/g) sodium fluoride (7.9 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "42c8ae03-7559-51a8-e063-6394a90ab69e", "openfda": {"unii": ["RGL5YE86CZ", "8ZYQ1474W7"], "rxcui": ["1297381"], "spl_set_id": ["efe3646d-9eb1-4a49-aeb4-c4c224056851"], "manufacturer_name": ["Dental Technologies, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "497 g in 1 BOTTLE (55346-0942-1)", "package_ndc": "55346-0942-1", "marketing_start_date": "20130401"}], "brand_name": "Alpha-Pro", "product_id": "55346-0942_42c8ae03-7559-51a8-e063-6394a90ab69e", "dosage_form": "GEL", "product_ndc": "55346-0942", "generic_name": "Sodium Fluoride and Hydrofluoric Acid", "labeler_name": "Dental Technologies, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alpha-Pro", "active_ingredients": [{"name": "HYDROFLUORIC ACID", "strength": "4.4 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "7.9 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20130401", "listing_expiration_date": "20261231"}