Home NDC 37808-167-72 HEB
Product NDC 37808-167
Requested package NDC 37808-167-72
11-digit product format 378080167
Labeler code 37808
Product ID 37808-167_47e5198e-7bfa-72a8-e063-6294a90a7ec5
Type HUMAN OTC DRUG
Nonproprietary name Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler HEB
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-12-01
Substance SODIUM FLUORIDE
Active strength .15 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 5 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 e2bbac7714bc…27bdfed8d636…
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 HEBuddy
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .15 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 416783 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-167-70 HEBHEBuddy 12 in 1 CASE PASTE, DENTIFRICE 12 7 37808-167-70 HEBHEBuddy 119 g in 1 TUBE PASTE, DENTIFRICE 119 7 37808-167-72 HEBHEBuddy 119 g in 1 TUBE PASTE, DENTIFRICE 119 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 FLUORIDE ION ACTIVE MOIETY Q80VPU408O HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 COCAMIDOPROPYL BETAINE INACTIVE INGREDIENT 5OCF3O11KX HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 HYDRATED SILICA INACTIVE INGREDIENT Y6O7T4G8P9 HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 POLYETHYLENE GLYCOL 600 INACTIVE INGREDIENT NL4J9F21N9 HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1 WATER INACTIVE INGREDIENT 059QF0KO0R HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-167 HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 5 Current NDC, Legacy NDC, 3 package rows 20250309_2c972c65-34aa-4348-b997-c5e65a884575.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 5 of 49 · 974 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 37808-167-72 37808016772 119 g in 1 TUBE (37808-167-72) 119 g 2012-12-01 No No Current