heb extra whitening
Generic: fluoride
Labeler: hebDrug Facts
Product Profile
Brand Name
heb extra whitening
Generic Name
fluoride
Labeler
heb
Dosage Form
PASTE, DENTIFRICE
Routes
Active Ingredients
potassium nitrate 5 g/100g, sodium fluoride .15 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
37808-681
Product ID
37808-681_441bb7e0-ebf7-602d-e063-6294a90aba7e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M022
Listing Expiration
2026-12-31
Marketing Start
2011-01-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808681
Hyphenated Format
37808-681
Supplemental Identifiers
RxCUI
UPC
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
heb extra whitening (source: ndc)
Generic Name
fluoride (source: ndc)
Application Number
M022 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 g/100g
- .15 g/100g
Packaging
- 1 TUBE in 1 CARTON (37808-681-29) / 113 g in 1 TUBE
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "441bb7e0-ebf7-602d-e063-6294a90aba7e", "openfda": {"upc": ["0041220819522"], "unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1038929"], "spl_set_id": ["9bdcbd3f-095b-43d1-8a8e-0ba3eab14e0e"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (37808-681-29) / 113 g in 1 TUBE", "package_ndc": "37808-681-29", "marketing_start_date": "20251121"}], "brand_name": "HEB Extra Whitening", "product_id": "37808-681_441bb7e0-ebf7-602d-e063-6294a90aba7e", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "37808-681", "generic_name": "Fluoride", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HEB", "brand_name_suffix": "Extra Whitening", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "5 g/100g"}, {"name": "SODIUM FLUORIDE", "strength": ".15 g/100g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}