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Dextromethorphan hydrobromide 4 MG/ML / guaifenesin 80 MG/ML Oral Solution — RxCUI 1113368

RxNorm drug concept · Semantic clinical drug
RxCUI 1113368 Semantic clinical drug · SCD ● Current RxNorm concept 3 FDA products 5 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

RxCUI1113368
Official nameDextromethorphan hydrobromide 4 MG/ML / guaifenesin 80 MG/ML Oral Solution
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asdextromethorphan hydrobromide 4 MG/ML / guaifenesin 80 MG/ML Syrup; dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 5 mL Oral Solution; dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG per 5 ML Oral Solution
FDA products mapped3
Package NDCs mapped5
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 won't necessarily silence your cough entirely, but it does temporarily suppress the cough reflex and reduce how intense and frequent your cough is. It can also help reduce that...
  • What exactly does dextromethorphan do — will it stop my cough completely?
  • It depends on your child's age and the specific product. Most dextromethorphan products should not be given to children under 4 years old without a doctor's guidance. Some products...
  • This is a really important question. If your antidepressant is an MAOI (monoamine oxidase inhibitor), you absolutely cannot take dextromethorphan — not while you're on it, and not...
📖 Read our full Dextromethorphan guide →

🕸️ Concept Web — How Dextromethorphan hydrobromide 4 MG/ML / guaifene... 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 4 MG/ML / guaifenesin 80 MG/ML Oral Solution RxCUI 1113368

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

  1. Ingredients 4

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

    • Dextromethorphan 3289
    • Guaifenesin 5032
    • Dextromethorphan / guaifenesin 214488
    • Dextromethorphan hydrobromide 102490
  2. Dose forms 9

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

    • Dextromethorphan / guaifenesin Oral Solution 371766
    • Dextromethorphan hydrobromide / guaifenesin Oral Solution 2647597
    • Dextromethorphan / guaifenesin Oral Liquid Product 1155190
    • Dextromethorphan / guaifenesin Oral Product 1155191
    • Dextromethorphan hydrobromide / guaifenesin Oral Liquid Product 2660140
    • Dextromethorphan hydrobromide / guaifenesin Oral Product 2663099
    • Oral Solution 316968
    • Oral Liquid Product 1151137
    • +1 more in this family
  3. Clinical & branded drugs 2

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

    • Dextromethorphan hydrobromide 4 MG/ML 1010978
    • Guaifenesin 80 MG/ML 331795

Showing up to 8 concepts per family — 14 of 15 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 4 MG/ML SCDC · 1010978
  • Guaifenesin 80 MG/ML SCDC · 331795
  • Dextromethorphan / guaifenesin Oral Solution SCDF · 371766
  • Dextromethorphan hydrobromide / guaifenesin Oral Solution SCDFP · 2647597
  • Dextromethorphan / guaifenesin Oral Liquid Product SCDG · 1155190
  • Dextromethorphan / guaifenesin Oral Product SCDG · 1155191
  • Dextromethorphan hydrobromide / guaifenesin Oral Liquid Product SCDGP · 2660140
  • Dextromethorphan hydrobromide / guaifenesin Oral Product SCDGP · 2663099

📦 FDA Products & Package NDCs

3 products · 5 package NDCs
5 package NDCs map to RxCUI 1113368 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
45737-0251-16 473 mL in 1 BOTTLE (45737-251-16) Bio-Z-Cough Advanced Generic Corporation 2012-07-01
52083-0400-01 30 mL in 1 BOTTLE, PLASTIC (52083-400-01) ZYNCOF Kramer Novis 2011-06-01
52083-0400-04 120 mL in 1 BOTTLE, PLASTIC (52083-400-04) ZYNCOF Kramer Novis 2011-06-01
52083-0400-16 474 mL in 1 BOTTLE, PLASTIC (52083-400-16) ZYNCOF Kramer Novis 2013-01-23
52083-0600-16 473 mL in 1 BOTTLE, PLASTIC (52083-600-16) G-ZYNCOF Kramer Novis 2012-12-03
Observed labelers: Kramer Novis (4) · Advanced Generic Corporation (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.