auraglow whitening

Generic: sodium fluoride

Labeler: auraglow llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name auraglow whitening
Generic Name sodium fluoride
Labeler auraglow llc
Dosage Form PASTE, DENTIFRICE
Routes
DENTAL
Active Ingredients

sodium fluoride 2.3 mg/g

Manufacturer
Auraglow LLC

Identifiers & Regulatory

Product NDC 81740-003
Product ID 81740-003_3f72b20e-32ad-468c-a67b-ff438c3a8396
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2025-10-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81740003
Hyphenated Format 81740-003

Supplemental Identifiers

RxCUI
1489127
UNII
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 auraglow whitening (source: ndc)
Generic Name sodium fluoride (source: ndc)
Application Number M021 (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 2.3 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (81740-003-03) / 113 g in 1 TUBE
source: ndc

Packages (1)

81740-003-03 1 TUBE in 1 CARTON (81740-003-03) / 113 g in 1 TUBE

Ingredients (1)

sodium fluoride (2.3 mg/g)

Linked Drug Pages (1)

Auraglow Whitening ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "3f72b20e-32ad-468c-a67b-ff438c3a8396", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["1489127"], "spl_set_id": ["9d45e436-92f6-4a9e-9b82-329847dca9ba"], "manufacturer_name": ["Auraglow LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (81740-003-03)  / 113 g in 1 TUBE", "package_ndc": "81740-003-03", "marketing_start_date": "20251020"}], "brand_name": "Auraglow Whitening", "product_id": "81740-003_3f72b20e-32ad-468c-a67b-ff438c3a8396", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "81740-003", "generic_name": "SODIUM FLUORIDE", "labeler_name": "Auraglow LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Auraglow Whitening", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "2.3 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251020", "listing_expiration_date": "20261231"}