anticavity
Generic: sodium fluoride
Labeler: your military exchangesDrug Facts
Product Profile
Brand Name
anticavity
Generic Name
sodium fluoride
Labeler
your military exchanges
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
55301-435
Product ID
55301-435_4aa3bb29-0444-1355-e063-6394a90a4609
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2015-06-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55301435
Hyphenated Format
55301-435
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 (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (55301-435-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4aa3bb29-0444-1355-e063-6394a90a4609", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["eb95e0ca-a94c-41cb-9f54-6c64ed9a9733"], "manufacturer_name": ["Your Military Exchanges"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (55301-435-43)", "package_ndc": "55301-435-43", "marketing_start_date": "20150628"}], "brand_name": "Anticavity", "product_id": "55301-435_4aa3bb29-0444-1355-e063-6394a90a4609", "dosage_form": "MOUTHWASH", "product_ndc": "55301-435", "generic_name": "Sodium fluoride", "labeler_name": "Your Military Exchanges", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".1 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150601", "listing_expiration_date": "20271231"}