anticavity fluoride rinse

Generic: sodium fluoride

Labeler: h e b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name anticavity fluoride rinse
Generic Name sodium fluoride
Labeler h e b
Dosage Form MOUTHWASH
Routes
ORAL
Active Ingredients

sodium fluoride 1 mg/mL

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-163
Product ID 37808-163_4b93abb5-e1e0-0fb5-e063-6294a90a6683
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2027-12-31
Marketing Start 2010-09-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808163
Hyphenated Format 37808-163

Supplemental Identifiers

RxCUI
1038904
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 fluoride rinse (source: ndc)
Generic Name sodium fluoride (source: ndc)
Application Number M021 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1000 mL in 1 BOTTLE, PLASTIC (37808-163-86)
source: ndc

Packages (1)

37808-163-86 1000 mL in 1 BOTTLE, PLASTIC (37808-163-86)

Ingredients (1)

sodium fluoride (1 mg/mL)

Linked Drug Pages (1)

Anticavity Fluoride Rinse ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b93abb5-e1e0-0fb5-e063-6294a90a6683", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["1038904"], "spl_set_id": ["87327a36-a314-4daa-83b6-b4bd3e26bba2"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (37808-163-86)", "package_ndc": "37808-163-86", "marketing_start_date": "20100929"}], "brand_name": "Anticavity Fluoride Rinse", "product_id": "37808-163_4b93abb5-e1e0-0fb5-e063-6294a90a6683", "dosage_form": "MOUTHWASH", "product_ndc": "37808-163", "generic_name": "SODIUM FLUORIDE", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity Fluoride Rinse", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "1 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100929", "listing_expiration_date": "20271231"}