basic care childrens allergy relief Loratadine 5 mg/5mL Solution
by Amazon.com Services LLC · 1 BOTTLE in 1 CARTON (72288-511-26) / 120 mL in 1 BOTTLE
NDC 72288-0511-26
🏷️ FDA NDC (as labeled)
72288-511-26
billing pads the product segment with a zero
This package
Contains120 mL in 1 bottle
Pack sizes2 compare ↓
Also comes in:
240 mL 72288-0511-34
OTC
Generic
Discontinued
Non-controlled
⚠ Discontinued by firm
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. 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)
72288-511-26
Product NDC
72288-511
11-digit billing NDC
72288051126
RxCUI
692783
UNII
7AJO3BO7QN
Application #
ANDA075728
SPL Set ID
90f40330-46a6-44cf-9b09-6f791c9b210b
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
Discontinued
FDA listing status
Discontinued by firm
Marketing start
2021-05-11
Route
ORAL
Dosage form
SOLUTION
Substance
LORATADINE
Why two NDCs?
The FDA registers this code as 72288-511-26 — 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 → 72288-0511-26. 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 Other antihistamines for systemic use class.
Drug family (ATC)
Other antihistamines for systemic use
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 holderL PERRIGO CO
FDA applicationANDA075728 (ANDA)
Labeler code72288
First marketedMay 2021
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
Loratadine is used to treat allergy symptoms: sneezing runny nose itching of the nose or throat red, itchy, or watery eyes Loratadine 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
- Loratadine is an antihistamine that temporarily relieves common allergy symptoms — things like a runny nose, sneezing, itchy or watery eyes, and an itchy nose or throat. It works f...
- When taken as directed, loratadine is considered non-drowsy for most people. However, if you take more than the recommended daily amount, drowsiness can happen. So stick to the dos...
- It depends on the age. Children 6 and older can take standard adult doses of most forms. Children 2 to under 6 can use the oral solution or chewable tablets, but at a lower amount....
- You should check with your doctor before taking loratadine if you have liver or kidney disease. Your doctor may need to adjust your dose. It's not necessarily off-limits, but it's...
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Loratadine — tap one for details:
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 Loratadine?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
FlavorGrape
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 7FLD91C86K
Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
-
UNII PDC6A3C0OX
Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
-
UNII D65DG142WK
Maltitol is a sugar alcohol made by hydrogenating maltose. It's used as a sweetener and filler in medicines to improve taste and add bulk to tablets and capsules.
-
UNII E4GA8884NN
Phosphoric acid is a weak mineral acid used in medicines as a buffer and pH adjuster. It helps stabilize the product and control its acidity level.
-
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 3980JIH2SW
A salt form of phosphoric acid that acts as a buffer and pH adjuster in medicines. It helps keep the product at the correct acidity level for stability and effectiveness.
-
UNII 506T60A25R
Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
-
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.
10 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesedetate disodium, glycerin, maltitol, monobasic sodium phosphate, natural and artificial grape flavor, phosphoric acid, propylene glycol, purified water, sodium benzoate, sorbitol, 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.
Try another pack size:
240 mL
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 |
|---|---|---|---|---|---|---|
| Good Sense childrens allergy relief 5 mg/5mL 00113-0671-26 | L. | 1 bottle | $0.041 | — | Availability likely | — |
| Childrens Loratadine Oral 5 mg/5mL 00904-6767-20 | Major | 1 bottle | $0.041 | — | Availability likely | — |
| Good Neighbor Pharmacy Childrens Loratadine 5 mg/5mL 24385-0531-26 | AmerisourceBergen | 1 bottle | $0.041 | — | Availability likely | — |
| good neighbor pharmacy childrens loratadine 5 mg/5mL 46122-0787-34 | Amerisource | 1 bottle | $0.041 | — | Availability likely | — |
| Loratadine 5 mg/5mL 54838-0558-40 | Lannett | 120 ml | $0.041 | — | Availability likely | — |
| Loratadine 5 mg/5mL 68001-0449-98 | BluePoint | 1 bottle | $0.041 | — | Availability likely | — |
| Loratadine 5 mg/5mL 69230-0322-12 | Camber | 1 bottle | $0.041 | — | Availability likely | — |
| leader childrens allergy relief 5 mg/5mL 70000-0473-01 | Cardinal | 1 bottle | $0.041 | — | Availability likely | — |
| Loratadine 5 mg/5mL 70677-1057-01 | STRATEGIC | 1 bottle | $0.041 | — | Availability likely | — |
| Childrens Loratadine Sugar Free 5 mg/5mL 70677-1058-01 | STRATEGIC | 1 bottle | $0.041 | — | Availability likely | — |
| Sunmark childrens loratadine 5 mg/5mL 49348-0636-34 | Strategic | 1 bottle | $0.042 | — | FDA listed | — |
| Loratadine 5 mg/5mL 70000-0125-01 | Cardinal | 1 bottle | $0.044 | — | Availability likely | — |
| good sense childrens allergy relief 5 mg/5mL 00113-1719-06 | L. | 1 bottle | — | — | FDA listed | — |
| Loratadine 5 mg/5mL 00363-0771-01 | WALGREEN | 1 bottle | — | — | FDA listed | — |
| Childrens Walitin 5 mg/5mL 00363-2108-08 | Walgreen | 1 bottle | — | — | FDA listed | — |
| Childrens Loratadine Sugar Free 5 mg/5mL 00363-2131-08 | Walgreen | 1 bottle | — | — | FDA listed | — |
| Claritin Allergy 1 mg/mL 11523-0101-01 | Bayer | 1 bottle | — | — | FDA listed | — |
| Children Claritin Allergy 5 mg/5mL 11523-4360-01 | Bayer | 1 bottle | — | — | FDA listed | — |
| childrens allergy relief 5 mg/5mL 11822-0620-00 | Rite | 1 bottle | — | — | FDA listed | — |
| Childrens Loratadine Oral 5 mg/5mL 17856-6767-01 | Atlantic | 72 cups | — | — | FDA listed | — |
| Loratadine 5 mg/5mL 21130-0042-24 | Better | 1 bottle | — | — | FDA listed | — |
| Good Neighbor Pharmacy Childrens Loratadine 5 mg/5mL 24385-0543-26 | AmerisourceBergen | 1 bottle | — | — | Discontinued | — |
| Loratadine 5 mg/5mL 30142-0062-24 | KROGER | 1 bottle | — | — | FDA listed | — |
| childrens allergy relief 5 mg/5mL 30142-0723-00 | Kroger | 1 bottle | — | — | Discontinued | — |
| topcare childrens allergy 5 mg/5mL 36800-0608-26 | Topco | 1 bottle | — | — | FDA listed | — |
| Childrens Loratadine Sugar Free 5 mg/5mL 37808-0131-08 | H | 1 bottle | — | — | FDA listed | — |
| Equaline Childrens Allergy Relief 5 mg/5mL 41163-0633-26 | United | 1 bottle | — | — | FDA listed | — |
| childrens allergy relief 5 mg/5mL 41250-0716-00 | Meijer, | 1 bottle | — | — | FDA listed | — |
| Childrens Loratadine Sugar Free 5 mg/5mL 41520-0131-08 | American | 1 bottle | — | — | FDA listed | — |
| Childrens Allergy 5 mg/5mL 49035-0538-08 | Wal-Mart | 1 bottle | — | — | FDA listed | — |
| equate childrens allergy 5 mg/5mL 49035-0611-34 | Wal-Mart | 1 bottle | — | — | FDA listed | — |
| Loratadine 5 mg/5mL 50090-1454-00 | A-S | 120 ml | — | — | FDA listed | — |
| Childrens Loratadine Oral 5 mg/5mL 50090-7516-00 | A-S | 1 bottle | — | — | FDA listed | — |
| Childrens Allergy Relief 5 mg/5mL 51316-0611-34 | CVS | 1 bottle | — | — | FDA listed | — |
| Childrens Loratadine 5 mg/5mL 51672-2073-04 | Sun | 1 bottle | — | — | FDA listed | — |
| Childrens Loratadine 5 mg/5mL 51672-2085-01 | Sun | 1 bottle | — | — | FDA listed | — |
| Childrens Loratadine Sugar Free 5 mg/5mL 51672-2108-01 | Sun | 1 bottle | — | — | FDA listed | — |
| Childrens Loratadine Sugar Free 5 mg/5mL 51672-2131-01 | Sun | 1 bottle | — | — | FDA listed | — |
| Loratadine 5 mg/5mL 54838-0554-40 | Lannett | 120 ml | — | — | FDA listed | — |
| dg health childrens allergy 5 mg/5mL 55910-0611-26 | Dolgencorp, | 1 bottle | — | — | FDA listed | — |
| childrens allergy 5 mg/5mL 56062-0092-08 | Publix | 1 bottle | — | — | FDA listed | — |
| Loratadine 5 mg/5mL 58602-0423-11 | Aurohealth | 1 bottle | — | — | FDA listed | — |
| Childrens Loratadine 5 mg/5mL 62011-0305-01 | Strategic | 1 bottle | — | — | FDA listed | — |
| welby childrens allergy relief 5 mg/5mL 64024-0023-26 | Aldi | 1 bottle | — | — | FDA listed | — |
| Good Sense childrens allergy relief 5 mg/5mL 68071-3904-04 | NuCare | 1 bottle | — | — | FDA listed | — |
| Loratadine 5 mg/5mL 68071-4451-04 | NuCare | 120 ml | — | — | FDA listed | — |
| Childrens Loratadine Sugar Free 5 mg/5mL 68788-8286-01 | Preferred | 1 bottle | — | — | FDA listed | — |
| Good Sense childrens allergy relief 5 mg/5mL 68788-8657-01 | Preferred | 1 bottle | — | — | FDA listed | — |
| Childrens Allergy 5 mg/5mL 69842-0337-26 | CVS | 1 bottle | — | — | FDA listed | — |
| Childrens Allergy 5 mg/5mL 69842-0535-08 | CVS | 1 bottle | — | — | FDA listed | — |
| basic care childrens allergy relief 5 mg/5mLthis 72288-0511-26 | Amazon.com | 1 bottle | — | — | Discontinued | — |
| Up And Up Childrens Allergy 5 mg/5mL 82442-0207-26 | Target | 1 bottle | — | — | FDA listed | — |
| childrens allergy relief 5 mg/5mL 72288-0533-34 | 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
🏛️
2021
On the market since
May 2021
📍
2026
Currently FDA-listed
5 years listed
🔓
·
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.
🔬 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 basic care childrens allergy relief (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 37%
Female · 63%
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 |
|---|---|---|---|
| 72288-0511-26 You're viewing this | 1 BOTTLE in 1 CARTON (72288-511-26) / 120 mL in 1 BOTTLE | 2021-05-11 | Discontinued by firm |
| 72288-0511-34 | 1 BOTTLE in 1 CARTON (72288-511-34) / 240 mL in 1 BOTTLE | 2021-05-18 | Active |
Pack size FAQ
What quantity is in NDC 72288-0511-26?
NDC 72288-0511-26 is listed by the FDA — 1 bottle in 1 carton / 120 ml in 1 bottle.
What NDC number is used to bill for this package of basic care childrens allergy relief Loratadine 5 mg/5mL Solution?
Bill NDC 72288-0511-26 — the 11-digit billing format is 72288051126. 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) | ✓ Available |
| Package photos | — Not published for this NDC No photo available yet for this listing. |
| 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.
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 72288-511-26, 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: 72288-0511-26, written without dashes as 72288051126. 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 72288-0511-26, the first segment (72288) is the labeler code FDA assigned to Amazon.com Services LLC; the middle segment (0511) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (26) 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 1 bottle (72288-0511-34). 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?
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 • itchy, watery eyes • sneezing • itching of the nose or throat
⏱️ Dosage and Administration ▾
Directions • use only with enclosed dosing cup adults and children 6 years and over 2 teaspoonfuls (tsp) daily; do not take more than 2 teaspoonfuls (tsp) in 24 hours children 2 to under 6 years of age 1 teaspoonful (tsp) daily; do not take more than 1 teaspoonful (tsp) in 24 hours children under 2 years of age ask a doctor consumers with liver or kidney disease ask a doctor Other information • do not use if carton is opened, or if printed neckband is broken or missing • store between 20° to 25°C (68° to 77°F)
⚠️ Warnings ▾
Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose. When using this product do not take more than directed.
Taking more than directed may cause drowsiness. Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.
If pregnant or breast feeding, 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 • do not use if carton is opened, or if printed neckband is broken or missing • store between 20° to 25°C (68° to 77°F)
🧪 Active Ingredient ▾
Active ingredient (in each 5 mL teaspoonful) Loratadine 5 mg
🧪 Inactive Ingredients ▾
Inactive ingredients edetate disodium, glycerin, maltitol, monobasic sodium phosphate, natural and artificial grape flavor, phosphoric acid, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose Questions or comments? 1-800-719-9260
🎯 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.