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⚪no package photo
in the FDA label

Allergy Relief D Cetirizine HCl, Pseudoephedrine HCl 5; 120 mg; mg Tablet, Extended Release

by Publix Super Markets Inc · 4 BLISTER PACK in 1 CARTON (56062-176-62) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
NDC 56062-0176-62
🏷️ FDA NDC (as labeled) 56062-176-62 billing pads the product segment with a zero
This package
Contains6 tablet, extended release in 1 blister pack Pack sizes2 compare ↓
Also comes in: 6 tablets 56062-0176-53
OTC Generic Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Jan 19, 2024 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Mar 2020. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 56062-176-62
Product NDC 56062-176
11-digit billing NDC 56062017662
NCPDP billing unit EA — each (per item)
Application # ANDA077170
Established class (EPC) Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist
DEA schedule Non-controlled
Marketing category ANDA
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Mar 2020)
Route ORAL
Dosage form TABLET, EXTENDED RELEASE
Substance CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
GCN Seq No 048415
GCN 13866
HICL code 022864
Ingredient (HICL) Cetirizine Hcl/Pseudoephedrine
HIC1 code Z
Therapeutic class — broad (HIC1) Body As A Whole
HIC2 code Z2
Therapeutic class — intermediate (HIC2) Antihistamines, Antiserotonins, Immunosuppressants
HIC3 code Z2O
Therapeutic class — specific (HIC3) 2Nd Gen Antihistamine And Decongestant Combination
AHFS code 04:08.00.00
AHFS class Second Generation Antihistamines
FDB label name PUB ALLERGY RELIEF-D TABLET
FDB brand name Allergy Relief-D
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 56062-176-62 — 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 → 56062-0176-62. 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.

🏭 Manufacturer & labeler

LabelerPublix Super Markets Inc
Application holderIVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
FDA applicationANDA077170 (ANDA)
Labeler code56062
Product typeHuman Otc Drug
Portfolio112 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

Label name PUB ALLERGY RELIEF-D TABLET Ingredient Cetirizine Hcl/Pseudoephedrine
📖 What it is MedlinePlus · NLM

Cetirizine injection is used to treat acute urticaria (sudden appearance of hives). 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.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • Great question. It's a two-in-one product. Cetirizine is an antihistamine that targets allergy symptoms like runny nose, sneezing, and itchy, watery eyes. Pseudoephedrine is a deco...
  • What exactly does this medication do — why does it have two ingredients?
  • No — please don't. These are extended-release tablets, which means they're specially designed to release medication slowly over 12 hours. Breaking or chewing the tablet can dump to...
  • Can I break the tablet in half if it's hard to swallow?
📖 Read our full Cetirizine / Pseudoephedrine guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

🧪 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.

We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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 systemPer eachPer 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.
Try another pack size: 6 tablets
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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
All Day Allergy D 5 mg/1; 120 mg 00113-2147-62 L. 1 tablet $0.563 — Availability likely —
Rugby Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride 5 mg/1; 120 mg 00536-1279-12 Rugby 1 tablet $0.563 — Availability likely —
Cetirizine hydrochloride and Pseudoephedrine hydrochloride 5 mg/1; 120 mg 45802-0147-53 Padagis 1 tablet $0.563 — Availability likely —
good neighbor pharmacy all day allergy d 5 mg/1; 120 mg 46122-0626-62 Amerisource 1 tablet $0.563 — Availability likely —
Leader Allergy Relief D 5 mg/1; 120 mg 70000-0042-01 Cardinal 1 tablet $0.563 — Availability likely —
Allergy relief-D 5 mg/1; 120 mg 70677-1020-01 STRATEGIC 6 tablets $0.563 — Availability likely —
Foster And Thrive All Day Allergy D 5 mg/1; 120 mg 70677-1311-01 Strategic 1 tablet $0.563 — Availability likely —
good sense all day allergy d 5 mg/1; 120 mg 00113-0147-53 L. 1 tablet — — Discontinued —
Wal-Zyr D 5 mg/1; 120 mg 00363-0989-12 Walgreen 6 tablets — — FDA listed —
allergy relief D12 5 mg/1; 120 mg 00363-4923-53 Walgreen 1 tablet — — FDA listed —
allergy relief-D 5 mg/1; 120 mg 11822-3009-00 Rite 1 tablet — — FDA listed —
Allergy relief-D 5 mg/1; 120 mg 11822-9994-01 RITE 6 tablets — — FDA listed —
signature care allergy relief d 5 mg/1; 120 mg 21130-0644-62 Safeway 1 tablet — — FDA listed —
all day allergy d 5 mg/1; 120 mg 30142-0450-62 Kroger 1 tablet — — FDA listed —
Allergy and Sinus Relief 5 mg/1; 120 mg 30142-0633-62 Kroger 1 tablet — — FDA listed —
topcare all day allergy d 5 mg/1; 120 mg 36800-0744-62 Topco 1 tablet — — FDA listed —
allergy relief d 5 mg/1; 120 mg 37808-0651-53 H 1 tablet — — FDA listed —
12 hour allergy d 5 mg/1; 120 mg 41250-0728-53 Meijer 1 tablet — — FDA listed —
Zyrtec-D 5 mg/1; 120 mg 50580-0719-12 Kenvue 6 tablets — — FDA listed —
ZYRTEC-D Allergy Plus Congestion 5 mg/1; 120 mg 50580-0728-12 Kenvue 6 tablets — — FDA listed —
Allergy Relief D12 5 mg/1; 120 mg 51316-0607-53 CVS 1 tablet — — FDA listed —
Allergy relief-D 5 mg/1; 120 mg 51660-0940-12 Ohm 6 tablets — — FDA listed —
allergy relief d 5 mg/1; 120 mg 56062-0147-53 Publix 1 tablet — — FDA listed —
Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride 5 mg/1; 120 mg 58602-0703-09 Aurohealth 2 tablets — — FDA listed —
Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride 5 mg/1; 120 mg 62756-0915-62 Sun 6 tablets — — FDA listed —
kirkland signature aller tec d 5 mg/1; 120 mg 63981-0147-62 Costco 1 tablet — — FDA listed —
Allergy relief-D 5 mg/1; 120 mg 68016-0531-24 CHAIN 24 tablets — — FDA listed —
allergy relief d 5 mg/1; 120 mg 69842-0415-53 CVS 1 tablet — — FDA listed —
Allergy Relief-D 5 mg/1; 120 mg 69842-0994-12 CVS 6 tablets — — FDA listed —
equate allergy relief d nasal decongestant 5 mg/1; 120 mg 79903-0126-14 WALMART 1 tablet — — FDA listed —
Allergy Relief D 5; 120 mg/1; mgthis 56062-0176-62 Publix 6 tablets — — Discontinued —
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
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
56062-0176-53 2 BLISTER PACK in 1 CARTON (56062-176-53) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 2010-03-11 Discontinued by firm
56062-0176-62 You're viewing this 4 BLISTER PACK in 1 CARTON (56062-176-62) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 2010-03-11 Discontinued by firm

Pack size FAQ

What quantity is in NDC 56062-0176-62?
NDC 56062-0176-62 is listed by the FDA — 4 blister pack in 1 carton / 6 tablet, extended release in 1 blister pack.
What NDC number is used to bill for this package of Allergy Relief D Cetirizine HCl, Pseudoephedrine HCl 5; 120 mg; mg Tablet, Extended Release?
Bill NDC 56062-0176-62 — the 11-digit billing format is 56062017662. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
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) — Not published for this NDC No structured label is linked to this listing in DailyMed/openFDA.
Package photos — Not published for this NDC The FDA label for this product carries no photos.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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.
Why is there no full label on this page?
No structured FDA label (SPL) is currently linked to this NDC in DailyMed/openFDA. That can happen with older listings, certain OTC and repackaged products, and recently updated listings whose label has not yet propagated. The listing itself is still valid — this page shows everything the public feeds provide for this package.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 56062-176-62, 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: 56062-0176-62, written without dashes as 56062017662. 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 56062-0176-62, the first segment (56062) is the labeler code FDA assigned to Publix Super Markets Inc; the middle segment (0176) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (62) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 6 tablets (56062-0176-53). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Publix Super Markets Inc 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.
📄 FDA label
📄 FDA label 19 words ▾

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
← 56062-0166-26 · Publix 56062-0188-16 · Publix →
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.