anticavity fluoride rinse
Generic: sodium fluoride
Labeler: h e bDrug Facts
Product Profile
Brand Name
anticavity fluoride rinse
Generic Name
sodium fluoride
Labeler
h e b
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
37808-213
Product ID
37808-213_4b93abb5-e1e2-0fb5-e063-6294a90a6683
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2016-06-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808213
Hyphenated Format
37808-213
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- .2 mg/mL
Packaging
- 532 mL in 1 BOTTLE, PLASTIC (37808-213-44)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b93abb5-e1e2-0fb5-e063-6294a90a6683", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["240698"], "spl_set_id": ["c68b0644-685d-4c62-bf5d-3a5bbea3b052"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "532 mL in 1 BOTTLE, PLASTIC (37808-213-44)", "package_ndc": "37808-213-44", "marketing_start_date": "20160621"}], "brand_name": "Anticavity Fluoride Rinse", "product_id": "37808-213_4b93abb5-e1e2-0fb5-e063-6294a90a6683", "dosage_form": "MOUTHWASH", "product_ndc": "37808-213", "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": ".2 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160621", "listing_expiration_date": "20271231"}