anticavity

Generic: sodium fluoride

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

Drug Facts

Product Profile

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

sodium fluoride .1 mg/mL

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-119
Product ID 37808-119_4b944151-684f-b456-e063-6394a90aac29
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2027-12-31
Marketing Start 2021-04-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808119
Hyphenated Format 37808-119

Supplemental Identifiers

RxCUI
313029
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
  • .1 mg/mL
source: ndc
Packaging
  • 1000 mL in 1 BOTTLE, PLASTIC (37808-119-86)
source: ndc

Packages (1)

37808-119-86 1000 mL in 1 BOTTLE, PLASTIC (37808-119-86)

Ingredients (1)

sodium fluoride (.1 mg/mL)

Linked Drug Pages (1)

Anticavity ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b944151-684f-b456-e063-6394a90aac29", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["8df324a7-9204-40f3-8ddb-1656286d7d4e"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (37808-119-86)", "package_ndc": "37808-119-86", "marketing_start_date": "20210420"}], "brand_name": "Anticavity", "product_id": "37808-119_4b944151-684f-b456-e063-6394a90aac29", "dosage_form": "RINSE", "product_ndc": "37808-119", "generic_name": "Sodium Fluoride", "labeler_name": "H E B", "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": "20210420", "listing_expiration_date": "20271231"}