Aluminum hydroxide 160 MG / magnesium hydroxide 105 MG Chewable Tablet — RxCUI 1376207
RxNorm drug concept · Semantic clinical drug
RxCUI 1376207
Semantic clinical drug · SCD
● Current RxNorm concept 1 FDA product
1 package NDC
Snapshot Jul 14, 2026
What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.
🗂️ Key Facts
RxCUI1376207
Official nameAluminum hydroxide 160 MG / magnesium hydroxide 105 MG Chewable Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
FDA products mapped1
Package NDCs mapped1
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Aluminum Hydroxide and Magnesium Hydroxide: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- It's designed to ease the discomfort of too much stomach acid. That includes acid indigestion, heartburn, sour stomach, and the upset stomach that comes along with those symptoms....
- What exactly does this antacid do — what symptoms will it help with?
- Give the bottle a good shake before every dose — that's important because the ingredients can settle. Adults and kids 12 and up take 2 to 4 teaspoonfuls up to four times a day, or...
- How do I take Mag-AL Liquid, and does it matter when I take it?
🕸️ Concept Web — How Aluminum hydroxide 160 MG / magnesium hydroxide... Connects
One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept
Aluminum hydroxide 160 MG / magnesium hydroxide 105 MG Chewable Tablet
RxCUI 1376207 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
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Ingredients 3
The active substance itself — no strength, form, or brand attached yet.
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Aluminum hydroxide
612IN -
Magnesium hydroxide
6581IN -
Aluminum hydroxide / magnesium hydroxide
1009149MIN
-
Aluminum hydroxide
-
Dose forms 8
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Aluminum hydroxide / magnesium hydroxide Chewable Tablet
370821SCDF -
Aluminum hydroxide / magnesium hydroxide Chewable Product
1294818SCDG -
Aluminum hydroxide / magnesium hydroxide Oral Product
1155638SCDG -
Aluminum hydroxide / magnesium hydroxide Pill
1155639SCDG -
Chewable Tablet
91058DF -
Chewable Product
1294716DFG -
Oral Product
1151131DFG -
Pill
1151133DFG
-
Aluminum hydroxide / magnesium hydroxide Chewable Tablet
-
Clinical & branded drugs 2
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Aluminum hydroxide 160 MG
315328SCDC -
Magnesium hydroxide 105 MG
1376206SCDC
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Aluminum hydroxide 160 MG
Showing up to 8 concepts per family — 13 of 13 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.
🔀 Generic ⇄ Brand Crosswalk
The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.
Generic (Clinical) Concepts
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Aluminum hydroxide 160 MG
SCDC · 315328 -
Magnesium hydroxide 105 MG
SCDC · 1376206 -
Aluminum hydroxide / magnesium hydroxide Chewable Tablet
SCDF · 370821 -
Aluminum hydroxide / magnesium hydroxide Chewable Product
SCDG · 1294818 -
Aluminum hydroxide / magnesium hydroxide Oral Product
SCDG · 1155638 -
Aluminum hydroxide / magnesium hydroxide Pill
SCDG · 1155639
📦 FDA Products & Package NDCs
1 product · 1 package NDC
1 package NDC map to RxCUI 1376207 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
| Package NDC | Package | Brand / generic name | Labeler | Marketing start |
|---|---|---|---|---|
| 30142-0610-00 | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (30142-610-00) | Kroger Extra Strength | THE KROGER CO., | 2019-05-16 |
Observed labelers:
THE KROGER CO., (1)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🗃️ Sources & Limits
Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
- A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
- Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
- Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
- Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.