Home NDC 37808-192 HEB
Product NDC 37808-192
11-digit product format 378080192
Labeler code 37808
Product ID 37808-192_437f93d5-d593-6b3a-e063-6294a90ac268
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 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 · 22 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 37808-192-00 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 37808-192-00 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 37808-192-00 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 37808-192-00 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 37808-192-00 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 37808-192-00 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 37808-192-00 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 37808-192-00 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 37808-192-00 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 37808-192-00 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 37808-192-00 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 37808-192-00 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 37808-192-02 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 37808-192-02 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 37808-192-02 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 37808-192-02 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 37808-192-02 I Inactivated by FDA 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 2026-12-31 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 891775 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-192-00 HEBHEBuddy 12 in 1 CASE PASTE, DENTIFRICE 12 9 37808-192-00 HEBHEBuddy 120 g in 1 TUBE PASTE, DENTIFRICE 120 9 37808-192-02 HEBHEBuddy 120 g in 1 TUBE PASTE, DENTIFRICE 120 9
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] 4 FLUORIDE ION ACTIVE MOIETY Q80VPU408O HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 COCAMIDOPROPYL BETAINE INACTIVE INGREDIENT 5OCF3O11KX HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 HYDRATED SILICA INACTIVE INGREDIENT Y6O7T4G8P9 HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 POLYETHYLENE GLYCOL 600 INACTIVE INGREDIENT NL4J9F21N9 HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 SORBITOL INACTIVE INGREDIENT 506T60A25R HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4 WATER INACTIVE INGREDIENT 059QF0KO0R HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-192 HEB HEBUDDY (FLUORIDE) PASTE, DENTIFRICE [HEB] 7 Current NDC, Legacy NDC, 3 package rows 20250119_a6af1baf-17bf-428c-8744-1490359b0cfb.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 34 of 50 · 995 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Hello Whipped Mellow Mint Dream Flavor SODIUM MONOFLUOROPHOSPHATE Colgate-Palmolive Company 7a72b687-475d-437a-9734-a29637e5516a 2025-11-11 Warnings Exact identifier application number: M021 Spry Dentifrice TOOTHPASTE Xlear Inc. 43567bbc-b07e-b605-e063-6294a90aad78 2025-11-11 Warnings Exact identifier application number: M021 Hello Naturally Whitening SODIUM MONOFLUOROPHOSPHATE COLGATE PALMOLIVE COMPANY 5ad241e1-6bfc-7863-6a7a-100753651f0a 2025-11-11 Warnings Exact identifier application number: M021 Hello Whipped Peppermint Stick Flavor SODIUM MONOFLUOROPHOSPHATE Colgate-Palmolive Company d6c4ac9e-f55e-4ebc-bd6a-e39eaeb4f813 2025-11-11 Warnings Exact identifier application number: M021 Super Mint MINT TOOTHPASTE SuperMouth, LLC. d23e89f5-7b65-4ed9-803a-38233f30d8f2 2025-11-07 Warnings Exact identifier application number: M021 Dentisse SODIUM FLUORIDE Dentisse, Inc. 326b290a-9bd2-468e-e054-00144ff8d46c 2025-11-04 Warnings Exact identifier application number: M021 Home Care Fluoride STANNOUS FLUORIDE Dental Technologies, Inc. 51f1d84c-809a-4c96-a117-7a8d8aa1e6b4 2025-11-04 Warnings Exact identifier application number: M021 Home Care Fluoride STANNOUS FLUORIDE Dental Technologies, Inc. c44686f8-93ee-4a8f-8481-3439d123f6d2 2025-11-04 Warnings Exact identifier application number: M021 Home Care Fluoride STANNOUS FLUORIDE Dental Technologies, Inc. 16ebcb37-5703-4e10-b965-570e18434b52 2025-11-04 Warnings Exact identifier application number: M021 Plak Smacker GREAT WHITE SHARK SODIUM FLUORIDE YOUNG PS ACQUISITION, LLC ca5b91aa-f69c-4553-a2b6-acf0ca1d920e 2025-11-04 Warnings Exact identifier application number: M021 Plak Smacker STANNOUS FLUORIDE Young Innovations, Inc. e65fa41e-ce2e-53e4-e053-2995a90a24d2 2025-11-04 Warnings Exact identifier application number: M021 Plak Smacker STANNOUS FLUORIDE Young Innovations, Inc. e65c62d9-e8a6-3101-e053-2995a90a1494 2025-11-04 Warnings Exact identifier application number: M021 Home Care Fluoride STANNOUS FLUORIDE Dental Technologies, Inc. 15bdc03e-2cc7-4b7d-96fc-4f3236ed5c75 2025-11-04 Warnings Exact identifier application number: M021 Strawberry Flavor Sodium Fluoride Anticavity Toothpast SODIUM FLUORIDE HISMILE PTY LTD 426c2aca-ca2b-5e34-e063-6294a90ae37c 2025-11-02 Warnings Exact identifier application number: M021 Watermelon Flavor Sodium Fluoride Anticavity Toothpast SODIUM FLUORIDE HISMILE PTY LTD 426e40cb-e30d-0db1-e063-6294a90a762b 2025-10-31 Warnings Exact identifier application number: M021 Classic Mint Flavor Sodium Fluoride Anticavity Toothpast SODIUM FLUORIDE HISMILE PTY LTD 425a9b71-5a7f-83e6-e063-6394a90ab703 2025-10-30 Warnings Exact identifier application number: M021 Grape Bubblegum Flavor Sodium Fluoride Anticavity Toothpast SODIUM FLUORIDE HISMILE PTY LTD 425b1a2e-7576-13a7-e063-6394a90aa865 2025-10-30 Warnings Exact identifier application number: M021 The Simpsons Pink Donut Flavor Sodium Fluoride Anticavity Toothpast SODIUM FLUORIDE HISMILE PTY LTD 426b8efa-e691-a67d-e063-6394a90abf8d 2025-10-30 Warnings Exact identifier application number: M021 Blue Raspberry Flavor Sodium Fluoride Anticavity Toothpast SODIUM FLUORIDE HISMILE PTY LTD 42583b32-525f-925d-e063-6294a90af76f 2025-10-29 Warnings Exact identifier application number: M021 PERIOE KAKAO KIDS Strawberry SODIUM FLUORIDE LG HOUSEHOLD & HEALTH CARE LTD. 4239f8c2-a5f5-3fa6-e063-6294a90acb47 2025-10-28 Warnings Exact identifier application number: M021
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 37808-192-00 37808019200 12 in 1 CASE Historical 37808-192-02 37808019202 120 g in 1 TUBE (37808-192-02) 120 g 2012-12-01 No No Current