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Dextromethorphan hydrobromide 1.33 MG/ML Oral Solution [Creomulsion] — RxCUI 1246340

RxNorm drug concept · Semantic branded drug
RxCUI 1246340 Semantic branded drug · SBD ● Current RxNorm concept 1 FDA product 1 package NDC Snapshot Jul 14, 2026

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Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

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

RxCUI1246340
Official nameDextromethorphan hydrobromide 1.33 MG/ML Oral Solution [Creomulsion]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asCreomulsion 20 MG per 15 ML Syrup; Creomulsion 20 MG in 15 mL Oral Solution; Creomulsion 1.33 MG/ML Oral Solution
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 Dextromethorphan: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • It's a cough suppressant. It temporarily relieves cough from minor throat and bronchial irritation, like with a cold or inhaled irritants. Some products also help you sleep by calm...
  • It depends on the product. Extended-release suspensions like Delsym are labeled for every 12 hours, while Giltuss Honey DM Cough is every 6 to 8 hours with a 4-dose daily limit. Ch...
  • Be careful. Don't use it if you take a prescription MAOI, or within 2 weeks of stopping one. If you're not sure whether your medicine is an MAOI, ask me or your doctor before takin...
  • Nighttime products can cause marked drowsiness, and children may become excitable. Avoid alcohol and be careful driving.
📖 Read our full Dextromethorphan guide →

🕸️ Concept Web — How Dextromethorphan hydrobromide 1.33 MG/ML Oral So... 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 Dextromethorphan hydrobromide 1.33 MG/ML Oral Solution [Creomulsion] RxCUI 1246340

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 2

    The active substance itself — no strength, form, or brand attached yet.

    • Dextromethorphan 3289
    • Dextromethorphan hydrobromide 102490
  2. Brand names 1

    The same medicine's trade names. A brand name alone says nothing about strength or form.

    • Creomulsion 687692
  3. Dose forms 13

    The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.

    • Dextromethorphan Oral Solution 371757
    • Dextromethorphan hydrobromide Oral Solution 2648076
    • Dextromethorphan Oral Liquid Product 1155546
    • Dextromethorphan Oral Product 1155547
    • Dextromethorphan hydrobromide Oral Liquid Product 2661829
    • Dextromethorphan hydrobromide Oral Product 2660147
    • Dextromethorphan Oral Solution [Creomulsion] 756558
    • Dextromethorphan hydrobromide Oral Solution [Creomulsion] 2657447
    • +5 more in this family
  4. Clinical & branded drugs 3

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

Showing up to 8 concepts per family — 14 of 19 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

  • Dextromethorphan hydrobromide 1.33 MG/ML Oral Solution SCD · 1246338
  • Dextromethorphan hydrobromide 1.33 MG/ML SCDC · 1246337
  • Dextromethorphan Oral Solution SCDF · 371757
  • Dextromethorphan hydrobromide Oral Solution SCDFP · 2648076
  • Dextromethorphan Oral Liquid Product SCDG · 1155546
  • Dextromethorphan Oral Product SCDG · 1155547
  • Dextromethorphan hydrobromide Oral Liquid Product SCDGP · 2661829
  • Dextromethorphan hydrobromide Oral Product SCDGP · 2660147

Brand-Name Concepts

  • Dextromethorphan hydrobromide 1.33 MG/ML [Creomulsion] SBDC · 1246339
  • Dextromethorphan Oral Solution [Creomulsion] SBDF · 756558
  • Dextromethorphan hydrobromide Oral Solution [Creomulsion] SBDFP · 2657447
  • Creomulsion Oral Liquid Product SBDG · 1172389
  • Creomulsion Oral Product SBDG · 1172390
  • Creomulsion BN · 687692

📦 FDA Products & Package NDCs

1 product · 1 package NDC
1 package NDC map to RxCUI 1246340 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
70893-0011-00 1 BOTTLE in 1 CARTON (70893-0011-0) / 118 mL in 1 BOTTLE (7... Creomulsion Cough Medicine Adult Formula Socius Care, LLC 2016-08-11
Observed labelers: Socius Care, LLC (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.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.