Home NDC 37808-681 HEB
Product NDC 37808-681
11-digit product format 378080681
Labeler code 37808
Product ID 37808-681_441bb7e0-ebf7-602d-e063-6294a90aba7e
Type HUMAN OTC DRUG
Nonproprietary name Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler HEB
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-01-20
Substance SODIUM FLUORIDE; POTASSIUM NITRATE
Active strength .15; 5 g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 37808-681 37808-681-19 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base HEB
Brand name suffix Extra Whitening
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .15 g/100g POTASSIUM NITRATE 5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup RU45X2JN0Z Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1038929 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-681-19 HEBExtra Whitening 113 g in 1 TUBE PASTE, DENTIFRICE 113 9 37808-681-19 HEBExtra Whitening 1 in 1 CARTON PASTE, DENTIFRICE 1 9 37808-681-29 HEBExtra Whitening 1 in 1 CARTON PASTE, DENTIFRICE 1 9 37808-681-29 HEBExtra Whitening 113 g in 1 TUBE PASTE, DENTIFRICE 113 9
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded POTASSIUM NITRATE ACTIVE INGREDIENT RU45X2JN0Z HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 FLUORIDE ION ACTIVE MOIETY Q80VPU408O HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 NITRATE ION ACTIVE MOIETY T93E9Y2844 HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 COCAMIDOPROPYL BETAINE INACTIVE INGREDIENT 5OCF3O11KX HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 HYDRATED SILICA INACTIVE INGREDIENT Y6O7T4G8P9 HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 POLYETHYLENE GLYCOL 400 INACTIVE INGREDIENT B697894SGQ HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 SODIUM METHYL COCOYL TAURATE INACTIVE INGREDIENT JVL98CG53G HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 SORBITOL INACTIVE INGREDIENT 506T60A25R HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 WATER INACTIVE INGREDIENT 059QF0KO0R HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2 XANTHAN GUM INACTIVE INGREDIENT TTV12P4NEE HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-681 HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB] 6 Current NDC, Legacy NDC, 4 package rows 20250119_9bdcbd3f-095b-43d1-8a8e-0ba3eab14e0e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 9 of 40 · 786 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 37808-681-19 37808068119 1 TUBE in 1 CARTON (37808-681-19) > 113 g in 1 TUBE 1 tube 2012-11-30 0000-00-00 No No Current 37808-681-29 37808068129 1 TUBE in 1 CARTON (37808-681-29) / 113 g in 1 TUBE 1 tube 2025-11-21 No No Current