Fexofenadine hydrochloride 6 MG/ML Oral Suspension [Allegra] — RxCUI 997493
RxNorm drug concept · Semantic branded drug
RxCUI 997493
Semantic branded drug · SBD
● Current RxNorm concept 2 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
RxCUI997493
Official nameFexofenadine hydrochloride 6 MG/ML Oral Suspension [Allegra]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asAllegra 6 MG/ML Oral Suspension; Allegra 30 MG in 5 mL Oral Suspension; Allegra 30 MG per 5 ML Oral Suspension
FDA products mapped2
Package NDCs mapped5
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?
🕸️ 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 [Allegra]
RxCUI 997493 Semantic branded drug · SBD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 2
The active substance itself — no strength, form, or brand attached yet.
-
Fexofenadine
87636IN -
Fexofenadine hydrochloride
236474PIN
-
Fexofenadine
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Allegra
324026BN
-
Allegra
-
Dose forms 13
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Fexofenadine Oral Suspension
670106SCDF -
Fexofenadine hydrochloride Oral Suspension
2647678SCDFP -
Fexofenadine Oral Liquid Product
1165010SCDG -
Fexofenadine Oral Product
1165011SCDG -
Fexofenadine hydrochloride Oral Liquid Product
2660330SCDGP -
Fexofenadine hydrochloride Oral Product
2662915SCDGP -
Fexofenadine Oral Suspension [Allegra]
670109SBDF -
Fexofenadine hydrochloride Oral Suspension [Allegra]
2657380SBDFP - +5 more in this family
-
Fexofenadine Oral Suspension
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Fexofenadine hydrochloride 6 MG/ML Oral Suspension
997491SCD -
Fexofenadine hydrochloride 6 MG/ML
997490SCDC -
Fexofenadine hydrochloride 6 MG/ML [Allegra]
997492SBDC
-
Fexofenadine hydrochloride 6 MG/ML Oral Suspension
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 [Allegra]
SBDC · 997492 -
Fexofenadine Oral Suspension [Allegra]
SBDF · 670109 -
Fexofenadine hydrochloride Oral Suspension [Allegra]
SBDFP · 2657380 -
Allegra Oral Liquid Product
SBDG · 1166659 -
Allegra Oral Product
SBDG · 1166660 -
Allegra
BN · 324026
📦 FDA Products & Package NDCs
2 products · 5 package NDCs
5 package NDCs map to RxCUI 997493 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 |
|---|---|---|---|---|
| 41167-4244-01 | 1 BOTTLE in 1 CARTON (41167-4244-1) / 240 mL in 1 BOTTLE | Childrens Allegra Allergy | Chattem, Inc. | 2011-03-03 |
| 41167-4244-04 | 1 BOTTLE in 1 CARTON (41167-4244-4) / 120 mL in 1 BOTTLE | Childrens Allegra Allergy | Chattem, Inc. | 2011-03-03 |
| 41167-4244-07 | 3 BOTTLE in 1 CELLO PACK (41167-4244-7) / 120 mL in 1 BOTTL... | Childrens Allegra Allergy | Chattem, Inc. | 2011-03-03 |
| 41167-4246-02 | 1 BOTTLE in 1 CARTON (41167-4246-2) / 240 mL in 1 BOTTLE | Childrens Allegra Allergy | Chattem, Inc. | 2023-03-01 |
| 41167-4246-04 | 1 BOTTLE in 1 CARTON (41167-4246-4) / 120 mL in 1 BOTTLE | Childrens Allegra Allergy | Chattem, Inc. | 2023-03-01 |
Observed labelers:
Chattem, Inc. (5)
— 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.