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Fexofenadine hydrochloride 6 MG/ML Oral Suspension [Wal-Fex] — RxCUI 1670344

RxNorm drug concept · Semantic branded drug
RxCUI 1670344 Semantic branded drug · SBD ● Current RxNorm concept 1 FDA product 2 package NDCs 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

RxCUI1670344
Official nameFexofenadine hydrochloride 6 MG/ML Oral Suspension [Wal-Fex]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asWal-Fex 6 MG/ML Oral Suspension; Wal-Fex 30 MG in 5 mL Oral Suspension; Wal-Fex 30 MG per 5 ML Oral Suspension
FDA products mapped1
Package NDCs mapped2
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

Our pharmacist-built guide to Fexofenadine: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • Fexofenadine is an antihistamine that relieves common allergy symptoms — things like a runny nose, sneezing, itchy or watery eyes, and an itchy nose or throat caused by hay fever o...
  • The FDA labels for fexofenadine do not list drowsiness as a side effect in the consumer sections provided. That said, everyone responds a little differently, so pay attention to ho...
  • You'll want to be careful here. The label says not to take fexofenadine at the same time as aluminum or magnesium antacids — the kind used for heartburn or upset stomach — and to a...
  • Can I take fexofenadine with my antacids or a glass of orange juice?
📖 Read our full Fexofenadine guide →

🕸️ Concept Web — How Fexofenadine hydrochloride 6 MG/ML Oral Suspensi... 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 Fexofenadine hydrochloride 6 MG/ML Oral Suspension [Wal-Fex] RxCUI 1670344

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.

    • Fexofenadine 87636
    • Fexofenadine hydrochloride 236474
  2. Brand names 1

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

    • Wal-Fex 1116525
  3. Dose forms 13

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

    • Fexofenadine Oral Suspension 670106
    • Fexofenadine hydrochloride Oral Suspension 2647678
    • Fexofenadine Oral Liquid Product 1165010
    • Fexofenadine Oral Product 1165011
    • Fexofenadine hydrochloride Oral Liquid Product 2660330
    • Fexofenadine hydrochloride Oral Product 2662915
    • Fexofenadine Oral Suspension [Wal-Fex] 1670342
    • Fexofenadine hydrochloride Oral Suspension [Wal-Fex] 2655675
    • +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

  • Fexofenadine hydrochloride 6 MG/ML Oral Suspension SCD · 997491
  • Fexofenadine hydrochloride 6 MG/ML SCDC · 997490
  • Fexofenadine Oral Suspension SCDF · 670106
  • Fexofenadine hydrochloride Oral Suspension SCDFP · 2647678
  • Fexofenadine Oral Liquid Product SCDG · 1165010
  • Fexofenadine Oral Product SCDG · 1165011
  • Fexofenadine hydrochloride Oral Liquid Product SCDGP · 2660330
  • Fexofenadine hydrochloride Oral Product SCDGP · 2662915

Brand-Name Concepts

  • Fexofenadine hydrochloride 6 MG/ML [Wal-Fex] SBDC · 1670341
  • Fexofenadine Oral Suspension [Wal-Fex] SBDF · 1670342
  • Fexofenadine hydrochloride Oral Suspension [Wal-Fex] SBDFP · 2655675
  • Wal-Fex Oral Liquid Product SBDG · 1670343
  • Wal-Fex Oral Product SBDG · 1187623
  • Wal-Fex BN · 1116525

📦 FDA Products & Package NDCs

1 product · 2 package NDCs
2 package NDCs map to RxCUI 1670344 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
00363-9230-04 1 BOTTLE, PLASTIC in 1 BOX (0363-9230-04) / 118 mL in 1 BOT... Dye Free Wal Fex childrens allergy Walgreens 2020-06-01
00363-9230-08 1 BOTTLE, PLASTIC in 1 BOX (0363-9230-08) / 237 mL in 1 BOT... Dye Free Wal Fex childrens allergy Walgreens 2020-06-01
Observed labelers: Walgreens (2) — 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.