Aluminum sulfate 8.42 MG/ML / calcium acetate 5.95 MG/ML Topical Solution — RxCUI 1250234
RxNorm drug concept · Semantic clinical drug
RxCUI 1250234
Semantic clinical drug · SCD
● Current RxNorm concept 4 FDA products
4 package NDCs
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
RxCUI1250234
Official nameAluminum sulfate 8.42 MG/ML / calcium acetate 5.95 MG/ML Topical Solution
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asaluminum sulfate 1347 MG / calcium acetate 952 MG per 160 ML Topical Solution; aluminum sulfate 1347 MG / calcium acetate 952 MG in 160 ML Topical Solution; (3 Packets (aluminum sulfate 1347 MG Powder / calcium acetate 952 MG Powder)) per 16 OZ Topical Solution
FDA products mapped4
Package NDCs mapped4
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Calcium Acetate: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- It's a fair question. Calcium acetate isn't being used here to boost your calcium — it's being used as a phosphate binder. When you take it with a meal, it grabs onto phosphate fro...
- What is calcium acetate actually doing for me — isn't calcium a normal supplement?
- Yes, timing with food is everything. You need to take it with each meal — not before, not hours after. The whole point is for it to be in your gut at the same time as the phosphate...
- When exactly should I take it — does it matter if I take it with food?
🕸️ Concept Web — How Aluminum sulfate 8.42 MG/ML / calcium acetate 5.... 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 sulfate 8.42 MG/ML / calcium acetate 5.95 MG/ML Topical Solution
RxCUI 1250234 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 sulfate
17621IN -
Calcium acetate
214342IN -
Aluminum sulfate / calcium acetate
705058MIN
-
Aluminum sulfate
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
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Domeboro
1293264BN
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Domeboro
-
Dose forms 6
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Aluminum sulfate / calcium acetate Topical Solution
1250233SCDF -
Aluminum sulfate / calcium acetate Topical Product
1250232SCDG -
Aluminum sulfate / calcium acetate Topical Solution [Domeboro]
1293266SBDF -
Domeboro Topical Product
1293267SBDG -
Topical Solution
316986DF -
Topical Product
1151122DFG
-
Aluminum sulfate / calcium acetate Topical Solution
-
Clinical & branded drugs 4
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Aluminum sulfate 8.42 MG/ML
1250230SCDC -
Calcium acetate 5.95 MG/ML
1250231SCDC -
Aluminum sulfate 8.42 MG/ML / calcium acetate 5.95 MG/ML Topical Solution [Domeboro]
1293268SBD -
Aluminum sulfate 8.42 MG/ML / calcium acetate 5.95 MG/ML [Domeboro]
1293265SBDC
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Aluminum sulfate 8.42 MG/ML
Showing up to 8 concepts per family — 14 of 14 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 sulfate 8.42 MG/ML
SCDC · 1250230 -
Calcium acetate 5.95 MG/ML
SCDC · 1250231 -
Aluminum sulfate / calcium acetate Topical Solution
SCDF · 1250233 -
Aluminum sulfate / calcium acetate Topical Product
SCDG · 1250232
Brand-Name Concepts
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Aluminum sulfate 8.42 MG/ML / calcium acetate 5.95 MG/ML Topical Solution [Domeboro]
SBD · 1293268 -
Aluminum sulfate 8.42 MG/ML / calcium acetate 5.95 MG/ML [Domeboro]
SBDC · 1293265 -
Aluminum sulfate / calcium acetate Topical Solution [Domeboro]
SBDF · 1293266 -
Domeboro Topical Product
SBDG · 1293267 -
Domeboro
BN · 1293264
📦 FDA Products & Package NDCs
4 products · 4 package NDCs
4 package NDCs map to RxCUI 1250234 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 |
|---|---|---|---|---|
| 16864-0140-01 | 12 POWDER, FOR SOLUTION in 1 PACKET (16864-140-01) | Kerasal Athletes Foot Rapid Symptom Relief Medicated Soak | Advantice Health, LLC. | 2012-06-26 |
| 16864-0240-01 | 12 POWDER, FOR SOLUTION in 1 BOX (16864-240-01) | Domeboro | Advantice Health, LLC. | 2012-06-26 |
| 63561-0178-02 | 12 PACKET in 1 CARTON (63561-0178-2) / 2299 mg in 1 PACKET... | Astringent | Granulation Technology, Inc. | 2025-06-12 |
| 81469-0999-12 | 12 PACKET in 1 BOX (81469-999-12) / 2299 mg in 1 PACKET (81... | Astringent Solution | First Nation Group | 2023-09-27 |
Observed labelers:
Advantice Health, LLC. (2) ·
First Nation Group (1) ·
Granulation Technology, Inc. (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.