Home NDC 37808-554 Antacid
Product NDC 37808-554
11-digit product format 378080554
Labeler code 37808
Product ID 37808-554_f6d20ce1-3ca8-4946-854c-368ced215e09
Type HUMAN OTC DRUG
Nonproprietary name aluminum hydroxide, magnesium hydroxide, simethicone
Dosage form LIQUID
Route ORAL
Labeler H E B
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-12-13
Substance ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE
Active strength 400; 400; 40 mg/10mL; mg/10mL; mg/10mL
Pharmacologic classes Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Skin Barrier Activity [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
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 Antacid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 400 mg/10mL MAGNESIUM HYDROXIDE 400 mg/10mL DIMETHICONE 40 mg/10mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QB0T2IUN0 Internal UNII lookup NBZ3QY004S Internal UNII lookup 92RU3N3Y1O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 307746 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-554-05 Antacid 355 mL in 1 BOTTLE LIQUID 355 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-554 ANTACID (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE) LIQUID [H E B] 3 Current NDC, Legacy NDC, 1 package rows 20241228_f294cf44-fb21-4b2e-8b7c-efd41416c6b2.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 25 of 34 · 678 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Calcium Carbonate 1250 mg CALCIUM CARBONATE CitraGen Pharmaceuticals, Inc. 766b3f3f-8bd1-281c-e053-2991aa0af54b 2025-01-30 Warnings Exact identifier application number: M001 Calcium Carbonate 10 gr (648 mg) CALCIUM CARBONATE CitraGen Pharmaceuticals, Inc. 723b940d-4f4b-f2e6-e053-2991aa0a8bcc 2025-01-30 Warnings Exact identifier application number: M001 Ultra Strength Antacid CALCIUM CARBONATE CVS 2bc4c71c-a9c5-17df-e063-6294a90ac88c 2025-01-27 Warnings Exact identifier application number: M001 Goodsense Ultra Strength Antacid CALCIUM CARBONATE Good Sense (Geiss, Destin & Dunn, Inc.) 492deace-7ea1-4fe3-a4c7-b2c6f195d68c 2025-01-20 Warnings Exact identifier application number: M001 Calcium Carbonate 10 gr (648 mg) (Antacid) CALCIUM CARBONATE 10GR (648 MG) Ulai Health LLC 641ae5b9-3bb6-41a1-ab12-367bf2fbcb0a 2025-01-20 Warnings Exact identifier application number: M001 GoodSense Extra Strength Antacid CALCIUM CARBONATE GoodSense 2fcdeb06-17de-49d8-97bb-8d31e1c0c61f 2025-01-20 Warnings Exact identifier application number: M001 HEB Extra Stregth Antacid CALCIUM CARBONATE H E B dcfe4c81-b6e0-4a9b-a521-f3ad0c0a8e48 2025-01-20 Warnings Exact identifier application number: M001 Aluminum Hydroxide, Magnesium Hydroxide and Simethicone ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE Everpharm LLC 2bda74cb-e77d-46bb-e063-6394a90af580 2025-01-16 Warnings Exact identifier application number: M001 Childrens Antacid CALCIUM CARBONATE CVS 1bf90c0c-b639-1c06-e063-6394a90ab85b 2025-01-16 Warnings Exact identifier application number: M001 Sodium Bicarbonate SODIUM BICARBONATE World Perfumes Inc a83544e4-ec09-1e95-e053-2995a90ab7b9 2025-01-15 Warnings Exact identifier application number: M001 Sodium Bicarbonate 10 gr SODIUM BICARBONATE Reliable 1 Laboratories LLC 321a772c-c44c-3d4e-e054-00144ff8d46c 2025-01-15 Warnings Exact identifier application number: M001 Calcium Carbonate 500 mg CALCIUM CARBONATE Reliable 1 Laboratories LLC 322f1b54-abe9-11a7-e054-00144ff8d46c 2025-01-15 Warnings Exact identifier application number: M001 Soothe Chewable CITRIC ACID Carolina Cannabis Creations LLC 04a27a71-b7b2-12aa-e063-6294a90a312f 2025-01-15 Warnings Exact identifier application number: M001 Soothe Chewable CITRIC ACID Carolina Cannabis Creations LLC 04a7720f-1e74-7578-e063-6394a90a5eae 2025-01-15 Warnings Exact identifier application number: M001 Soothe Chewable CITRIC ACID Carolina Cannabis Creations LLC 04a78060-7f0d-c4bd-e063-6294a90ae152 2025-01-15 Warnings Exact identifier application number: M001 Soothe Chewable CITRIC ACID Carolina Cannabis Creations LLC 04a78a5c-e3b5-f362-e063-6394a90a0807 2025-01-15 Warnings Exact identifier application number: M001 Rolaids Extra Strength Mint CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE Chattem, Inc. 604d79f3-cdfa-45e2-8c20-fa6e0ff09b2e 2025-01-15 Warnings Exact identifier application number: M001 Extra Strength Smooth Antacid CALCIUM CARBONATE H E B 19a3221f-e0c1-c47a-e063-6394a90a1f01 2025-01-14 Warnings Exact identifier application number: M001 Childrens Stomach Relief Antacid CALCIUM CARBONATE H E B 18fae1aa-1001-8035-e063-6394a90adc66 2025-01-14 Warnings Exact identifier application number: M001 Calcium Carbonate 10 gr (648 mg) (Antacid) CALCIUM CARBONATE 10GR (648 MG) Aphena Pharma Solutions - Tennessee, LLC ac839363-94fd-4c60-b5b6-70e4488ce1dd 2025-01-09 Warnings Exact identifier application number: M001
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 37808-554-05 37808055405 355 mL in 1 BOTTLE (37808-554-05) 355 ml 2021-12-13 0000-00-00 No No Current