anticavity

Generic: sodium fluoride

Labeler: target corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name anticavity
Generic Name sodium fluoride
Labeler target corporation
Dosage Form RINSE
Routes
ORAL
Active Ingredients

sodium fluoride .2 mg/mL

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-004
Product ID 11673-004_4b1dd4df-4c3d-c4fb-e063-6294a90a25e0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2027-12-31
Marketing Start 2011-08-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673004
Hyphenated Format 11673-004

Supplemental Identifiers

RxCUI
240698
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 anticavity (source: ndc)
Generic Name sodium fluoride (source: ndc)
Application Number M021 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/mL
source: ndc
Packaging
  • 500 mL in 1 BOTTLE, PLASTIC (11673-004-77)
source: ndc

Packages (1)

Ingredients (1)

sodium fluoride (.2 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b1dd4df-4c3d-c4fb-e063-6294a90a25e0", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["240698"], "spl_set_id": ["abfc1973-60ab-44e5-8147-33739d8bd7a3"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE, PLASTIC (11673-004-77)", "package_ndc": "11673-004-77", "marketing_start_date": "20110826"}], "brand_name": "Anticavity", "product_id": "11673-004_4b1dd4df-4c3d-c4fb-e063-6294a90a25e0", "dosage_form": "RINSE", "product_ndc": "11673-004", "generic_name": "Sodium fluoride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".2 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110826", "listing_expiration_date": "20271231"}