evo sensitive whitening anti-cavity fluoride

Generic: sodium fluoride

Labeler: ashtel studios, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name evo sensitive whitening anti-cavity fluoride
Generic Name sodium fluoride
Labeler ashtel studios, inc.
Dosage Form MOUTHWASH
Routes
ORAL
Active Ingredients

sodium fluoride .05 g/100mL

Manufacturer
Ashtel Studios, Inc.

Identifiers & Regulatory

Product NDC 70108-210
Product ID 70108-210_cdc9d79b-c80c-443e-9c18-71dfd970cc76
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2025-07-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70108210
Hyphenated Format 70108-210

Supplemental Identifiers

RxCUI
240698
UPC
0810147886081
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 evo sensitive whitening anti-cavity fluoride (source: ndc)
Generic Name sodium fluoride (source: ndc)
Application Number M021 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .05 g/100mL
source: ndc
Packaging
  • 296 mL in 1 BOTTLE (70108-210-01)
source: ndc

Packages (1)

Ingredients (1)

sodium fluoride (.05 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cdc9d79b-c80c-443e-9c18-71dfd970cc76", "openfda": {"upc": ["0810147886081"], "unii": ["8ZYQ1474W7"], "rxcui": ["240698"], "spl_set_id": ["1620c7fa-2af6-4462-af5d-9e122942788a"], "manufacturer_name": ["Ashtel Studios, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "296 mL in 1 BOTTLE (70108-210-01)", "package_ndc": "70108-210-01", "marketing_start_date": "20250710"}], "brand_name": "evo SENSITIVE WHITENING ANTI-CAVITY FLUORIDE", "product_id": "70108-210_cdc9d79b-c80c-443e-9c18-71dfd970cc76", "dosage_form": "MOUTHWASH", "product_ndc": "70108-210", "generic_name": "Sodium Fluoride", "labeler_name": "Ashtel Studios, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "evo SENSITIVE WHITENING ANTI-CAVITY FLUORIDE", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".05 g/100mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250710", "listing_expiration_date": "20261231"}