Home NDC 37808-336 HEB Enamel Protection
Product NDC 37808-336
11-digit product format 378080336
Labeler code 37808
Product ID 37808-336_441c1004-fd5d-d250-e063-6294a90aae44
Type HUMAN OTC DRUG
Nonproprietary name Potassium nitrate, sodium fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler HEB
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-02-20
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 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 Enamel Protection
Brand name suffix Multi Action
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 1038841 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 37808-336-19 HEB Enamel ProtectionMulti Action 113 g in 1 TUBE PASTE, DENTIFRICE 113 14 37808-336-19 HEB Enamel ProtectionMulti Action 1 in 1 CARTON PASTE, DENTIFRICE 1 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-336 HEB ENAMEL PROTECTION MULTI ACTION (POTASSIUM NITRATE, SODIUM FLUORIDE) PASTE, DENTIFRICE [HEB] 12 Current NDC, Legacy NDC, 2 package rows 20250119_8255de83-aa60-b081-e053-2a91aa0afcdc.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 37808-336-19 37808033619 1 TUBE in 1 CARTON (37808-336-19) / 113 g in 1 TUBE 1 tube 2019-02-20 0000-00-00 No No Current