Home NDC 37808-510 HEB Extra Strength
Product NDC 37808-510
11-digit product format 378080510
Labeler code 37808
Product ID 37808-510_bc8f027b-369d-4296-bd48-e6e12d5e79a1
Type HUMAN OTC DRUG
Nonproprietary name aluminum hydroxide and magnesium carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler HEB
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-03-20
Substance ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE
Active strength 160; 105 mg/1; mg/1
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 · 8 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 37808-510-10 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 37808-510-10 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 37808-510-10 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 37808-510-10 1332a3947898…d4bfe170f9cd…
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 Extra Strength
Brand name suffix Cherry Flavor
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 160 mg/1 MAGNESIUM CARBONATE 105 mg/1
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 37808-510-10 HEB Extra StrengthCherry Flavor 100 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 100 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-510 HEB EXTRA STRENGTH CHERRY FLAVOR (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE) TABLET, CHEWABLE [HEB] 4 Current NDC, Legacy NDC, 1 package rows 20240919_6e10ad65-5baf-4763-befe-ed046bf914b5.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 10 of 34 · 678 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 37808-510-10 37808051010 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (37808-510-10) 2019-03-20 0000-00-00 No No Current