therabreath anticavity

Generic: sodium fluoride

Labeler: church & dwight co., inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name therabreath anticavity
Generic Name sodium fluoride
Labeler church & dwight co., inc.
Dosage Form RINSE
Routes
ORAL
Active Ingredients

sodium fluoride .002 mg/10mL

Manufacturer
Church & Dwight Co., Inc.

Identifiers & Regulatory

Product NDC 10237-265
Product ID 10237-265_3e626c65-3a8b-ec3c-e063-6394a90ad8f4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2024-08-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10237265
Hyphenated Format 10237-265

Supplemental Identifiers

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 therabreath anticavity (source: ndc)
Generic Name sodium fluoride (source: ndc)
Application Number M021 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .002 mg/10mL
source: ndc
Packaging
  • 1000 mL in 1 BOTTLE, PLASTIC (10237-265-01)
  • 2 BOTTLE in 1 PACKAGE (10237-265-21) / 1000 mL in 1 BOTTLE
source: ndc

Packages (2)

Ingredients (1)

sodium fluoride (.002 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e626c65-3a8b-ec3c-e063-6394a90ad8f4", "openfda": {"unii": ["8ZYQ1474W7"], "spl_set_id": ["3c5d58f1-ea8c-4708-bbc6-21e1cd1446da"], "manufacturer_name": ["Church & Dwight Co., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (10237-265-01)", "package_ndc": "10237-265-01", "marketing_start_date": "20240815"}, {"sample": false, "description": "2 BOTTLE in 1 PACKAGE (10237-265-21)  / 1000 mL in 1 BOTTLE", "package_ndc": "10237-265-21", "marketing_start_date": "20260101"}], "brand_name": "TheraBreath Anticavity", "product_id": "10237-265_3e626c65-3a8b-ec3c-e063-6394a90ad8f4", "dosage_form": "RINSE", "product_ndc": "10237-265", "generic_name": "Sodium Fluoride", "labeler_name": "Church & Dwight Co., Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TheraBreath Anticavity", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".002 mg/10mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240815", "listing_expiration_date": "20261231"}