alcohol-free anticavity

Generic: sodium fluoride

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

Drug Facts

Product Profile

Brand Name alcohol-free anticavity
Generic Name sodium fluoride
Labeler h e b
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

sodium fluoride .1 mg/mL

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-942
Product ID 37808-942_4b93e61b-2f19-4421-e063-6394a90ae3f3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2027-12-31
Marketing Start 2017-01-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808942
Hyphenated Format 37808-942

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 alcohol-free 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 (37808-942-86)
source: ndc

Packages (1)

37808-942-86 1000 mL in 1 BOTTLE, PLASTIC (37808-942-86)

Ingredients (1)

sodium fluoride (.1 mg/mL)

Linked Drug Pages (1)

Alcohol-Free Anticavity ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b93e61b-2f19-4421-e063-6394a90ae3f3", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["8d40f693-083c-4eb6-9da1-42675d757e0e"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (37808-942-86)", "package_ndc": "37808-942-86", "marketing_start_date": "20170117"}], "brand_name": "Alcohol-Free Anticavity", "product_id": "37808-942_4b93e61b-2f19-4421-e063-6394a90ae3f3", "dosage_form": "LIQUID", "product_ndc": "37808-942", "generic_name": "Sodium fluoride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol-Free Anticavity", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".1 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170117", "listing_expiration_date": "20271231"}