CHILDRENS ALL DAY ALLERGY Cetirizine HCl 5 mg/5mL Solution
by Amazon.com Services LLC · 1 BOTTLE in 1 CARTON (72288-818-34) / 240 mL in 1 BOTTLE (72288-818-00)
NDC 72288-0818-34
🏷️ FDA NDC (as labeled)
72288-818-34
billing pads the product segment with a zero
OTC
Generic
On market
Non-controlled
🗂️ Data synced Aug 20, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
72288-818-34
Product NDC
72288-818
11-digit billing NDC
72288081834
RxCUI
1014673
UNII
64O047KTOA
Application #
ANDA204226
SPL Set ID
f9b17231-1787-4726-8e19-cf3430dd811c
Established class (EPC)
Histamine-1 Receptor Antagonist
Mechanism of action
Histamine H1 Receptor Antagonists
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-06-04
Route
ORAL
Dosage form
SOLUTION
Substance
CETIRIZINE HYDROCHLORIDE
Why two NDCs?
The FDA registers this code as 72288-818-34 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 72288-0818-34. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
🏷️ RxNorm drug class
This medicine belongs to the Histamine-1 Receptor Antagonist class.
Pharmacologic class
Histamine-1 Receptor Antagonist
Drug family (ATC)
Piperazine derivatives, Other antiallergics
How it works
Histamine H1 Receptor Antagonists
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
🏭 Manufacturer & labeler
LabelerAmazon.com Services LLC
Application holderPERRIGO R AND D CO
FDA applicationANDA204226 (ANDA)
Labeler code72288
First marketedJun 2026
Product typeHuman Otc Drug
Portfolio335 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.
🩺 Clinical
📖 What it is MedlinePlus · NLM
Cetirizine is used to treat allergy symptoms: sneezing runny nose itching of the nose or throat red, itchy, or watery eyes Cetirizine is also used to treat urticaria (hives; itchy raised red bumps on skin). Cetirizine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms. Cetirizine is also available in combination with pseudoephedrine. This monograph only includes information about the use of cetirizine alone. If you are taking the cetirizine and pseudoephedrine combination product, read th...
Read the full MedlinePlus article ↗📗 Our plain-language guide HelloPharmacist
- Cetirizine is an antihistamine that helps with allergies and hives. Most oral products — tablets, capsules, solutions — treat classic allergy symptoms like runny nose, sneezing, it...
- It can, yes — drowsiness is the most commonly reported side effect. Cetirizine is considered less sedating than older antihistamines because it doesn't penetrate the brain as readi...
- You can take oral cetirizine with or without food — it doesn't matter much. Food doesn't reduce the total amount absorbed, though it can delay the peak effect by an hour or two. So...
- Can I take cetirizine with food, or does it need to be on an empty stomach?
Patient education
Supplement & herbal interactions
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
💬 Questions about Cetirizine HCl?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
Yellow
FlavorBubble Gum
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
🧪 Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII XF417D3PSL
Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
-
UNII 6DC9Q167V3
Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
-
UNII OJ245FE5EU
Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
-
UNII 8KW3E207O2
A liquid sweetener made from sorbitol, a sugar alcohol derived from glucose. It sweetens the medicine and also acts as a humectant to help retain moisture and improve texture in liquid formulations.
-
UNII 96K6UQ3ZD4
Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.
-
UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
6 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesanhydrous citric acid, artificial bubble gum flavor, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed —
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
💲 Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per mL | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| foster and thrive childrens allergy relief 5 mg/5mL 70677-1042-01 | Strategic | 1 bottle | $0.035 | — | Availability likely | — |
| Good Neighbor Pharmacy Childrens All Day Allergy 5 mg/5mL 46122-0203-26 | Amerisource | 1 bottle | $0.035 | — | Availability likely | — |
| Leader Childrens All Day Allergy 5 mg/5mL 70000-0214-01 | Cardinal | 1 bottle | $0.037 | — | Availability likely | — |
| childrens cetirizine hydrochloride 5 mg/5mL 00904-6765-20 | Major | 1 bottle | $0.037 | — | Availability likely | — |
| Good Sense Childrens All Day Allergy 5 mg/5mL 00113-0189-26 | L. | 1 bottle | $0.037 | — | Availability likely | — |
| Good Sense Childrens All Day Allergy 5 mg/5mL 00113-0503-26 | L. | 1 bottle | $0.037 | — | Availability likely | — |
| Leader Childrens all day allergy 5 mg/5mL 70000-0215-01 | Cardinal | 1 bottle | $0.037 | — | Availability likely | — |
| Dye Free Childrens Cetirizine Hydrocholride 5 mg/5mL 68094-0004-62 | Precision | 10 cups | $0.447 | — | Availability likely | — |
| Signature Care Childrens Allergy Relief 5 mg/5mL 21130-0189-34 | Safeway | 1 bottle | — | — | Discontinued | — |
| Signature Care Childrens Allergy Relief 5 mg/5mL 21130-0475-26 | Safeway | 1 bottle | — | — | Discontinued | — |
| childrens all day allergy 5 mg/5mL 30142-0189-26 | Kroger | 1 bottle | — | — | FDA listed | — |
| Topcare Childrens All Day Allergy 5 mg/5mL 36800-0189-26 | Topco | 1 bottle | — | — | FDA listed | — |
| DG Health Childrens All Day Allergy 5 mg/5mL 55910-0714-26 | Dolgencorp, | 1 bottle | — | — | FDA listed | — |
| childrens cetirizine hydrochloride 5 mg/5mL 71205-0722-04 | Proficient | 1 bottle | — | — | FDA listed | — |
| Basic Care Childrens All Day Allergy 5 mg/5mL 72288-0330-34 | Amazon.com | 1 bottle | — | — | FDA listed | — |
| Kirkland Signature Childrens Aller Tec 5 mg/5mL 63981-0475-43 | Costco | 2 bottles | — | — | FDA listed | — |
| childrens all day allergy 5 mg/5mL 42507-0475-26 | HyVee | 1 bottle | — | — | FDA listed | — |
| basic care childrens all day allergy 5 mg/5mL 72288-0475-34 | Amazon.com | 1 bottle | — | — | FDA listed | — |
| careone childrens allergy relief 5 mg/5mL 41520-0301-26 | American | 1 bottle | — | — | FDA listed | — |
| Childrens All Day Allergy 5 mg/5mL 42507-0203-26 | HyVee | 1 bottle | — | — | FDA listed | — |
| Good Sense Childrens All Day Allergy 5 mg/5mL 50090-7068-00 | A-S | 1 bottle | — | — | FDA listed | — |
| childrens allergy relief 5 mg/5mL 11822-1189-00 | Rite | 1 bottle | — | — | FDA listed | — |
| Childrens All Day Allergy 5 mg/5mL 30142-0475-26 | Kroger | 1 bottle | — | — | FDA listed | — |
| childrens dye free allergy relief 5 mg/5mL 30142-0689-26 | Kroger | 1 bottle | — | — | FDA listed | — |
| TopCare Childrens All Day Allergy 5 mg/5mL 36800-0475-00 | Topco | 1 bottle | — | — | FDA listed | — |
| careone childrens allergy relief 5 mg/5mL 41520-0902-26 | American | 1 bottle | — | — | FDA listed | — |
| childrens cetirizine hydrochloride 5 mg/5mL 17856-6765-01 | ATLANTIC | 72 cups | — | — | FDA listed | — |
| childrens dye free allergy relief 5 mg/5mL 30142-0643-26 | Kroger | 1 bottle | — | — | FDA listed | — |
| Childrens Allergy Relief 5 mg/5mL 59779-0509-26 | CVS | 1 bottle | — | — | FDA listed | — |
| Equaline childrens all day allergy 5 mg/5mL 41163-0475-26 | United | 1 bottle | — | — | FDA listed | — |
| childrens cetirizine hydrochloride 5 mg/5mL 68788-8188-01 | Preferred | 1 bottle | — | — | FDA listed | — |
| Good Sense Childrens All Day Allergy 5 mg/5mL 68788-8803-01 | Preferred | 1 bottle | — | — | FDA listed | — |
| Childrens 24 Hour Allergy 5 mg/5mL 41250-0189-26 | Meijer | 1 bottle | — | — | FDA listed | — |
| childrens allergy relief 5 mg/5mL 11822-0475-00 | Rite | 1 bottle | — | — | FDA listed | — |
| Childrens 24 Hour Allergy 5 mg/5mL 41250-0475-26 | Meijer | 1 bottle | — | — | FDA listed | — |
| Good Sense Childrens All Day Allergy 5 mg/5mL 68788-4093-01 | Preferred | 1 bottle | — | — | FDA listed | — |
| allergy relief childrens 5 mg/5mL 59779-0837-26 | CVS | 1 bottle | — | — | FDA listed | — |
| Childrens All Day Allergy 5 mg/5mLthis 72288-0818-34 | Amazon.com | 1 bottle | — | — | FDA listed | — |
| Childrens All Day Allergy 5 mg/5mL 72288-0982-34 | Amazon.com | 1 bottle | — | — | FDA listed | — |
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.
⏳ Availability & generic status
🏛️
2026
On the market since
Jun 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug
This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
📊 Medicare Part D spend CMS · PART D · 2026 (Q1)
Medicare Part D (outpatient prescription) spending for Quzyttir (matched by generic name) — the program that covers self-administered drugs. 1 manufacturer.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Quzyttir. CMS lists 3 products for this generic; we show the highest-spend one. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$402.6K
Claims incl. refills
69
Beneficiaries
17
Spend / beneficiary
$23,680.41
Spend / claim
$5,834.30
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Cetirizine HCl — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 35%
Female · 65%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 72288-0818-34 You're viewing this | 1 BOTTLE in 1 CARTON (72288-818-34) / 240 mL in 1 BOTTLE (72288-818-00) | 2026-06-04 | Active |
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 72288-818-34, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 72288-0818-34, written without dashes as 72288081834. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 72288-0818-34, the first segment (72288) is the labeler code FDA assigned to Amazon.com Services LLC; the middle segment (0818) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (34) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Amazon.com Services LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Amazon.com Services LLC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
📄 FDA label — Drug Facts FDA SPL
The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • sneezing • itchy, watery eyes • itching of the nose or throat
⏱️ Dosage and Administration ▾
Directions • use only with enclosed dosing cup • find right dose on chart below • mL = milliliter adults and children 6 years and over 5 mL or 10 mL once daily depending upon severity of symptoms; do not take more than 10 mL in 24 hours. adults 65 years and over 5 mL once daily; do not take more than 5 mL in 24 hours. children 2 to under 6 years of age 2.5 mL once daily. If needed, dose can be increased to a maximum of 5 mL once daily or 2.5 mL every 12 hours. Do not give more than 5 mL in 24 hours. children under 2 years of age ask a doctor consumers with liver or kidney disease ask a doctor
⚠️ Warnings ▾
Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine. Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.
Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives. When using this product • drowsiness may occur • avoid alcoholic drinks • alcohol, sedatives, and tranquilizers may increase drowsiness • be careful when driving a motor vehicle or operating machinery Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.
If pregnant or breast-feeding: • if breast-feeding: not recommended • if pregnant: ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
(1-800-222-1222)
📦 Storage and Handling ▾
Other information • store between 20 ° -25 ° C (68 ° -77 ° F) • do not use if carton is opened, or if printed neckband is broken or missing • see bottom panel for lot number and expiration date
🧪 Active Ingredient ▾
Active ingredient (in each 5 mL) Cetirizine HCl 5 mg
🧪 Inactive Ingredients ▾
Inactive ingredients anhydrous citric acid, artificial bubble gum flavor, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose
🎯 Purpose ▾
Purpose Antihistamine
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.