Good Sense childrens allergy relief Loratadine 5 mg/5mL Solution — NDC 68071-3904-4 (Billing 68071-3904-04)
by NuCare Pharmaceuticals,Inc. · 1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE
This is a package of Good Sense childrens allergy relief Loratadine 5 mg/5mL Solution from NuCare Pharmaceuticals,Inc., marketed since Aug 2020 and currently FDA-listed. It is this product's only package size.
NDC 68071-3904-04
🏷️ FDA NDC (as labeled)
68071-3904-4
billing pads the package segment with a zero
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
68071-3904-4
Product NDC
68071-3904
11-digit billing NDC
68071390404
RxCUI
692783
UNII
7AJO3BO7QN
UPC
0368071390445
Application #
ANDA075728
SPL Set ID
40d25cdf-b63f-d5c9-e063-6394a90af509
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2020-08-02
Route
ORAL
Dosage form
SOLUTION
Substance
LORATADINE
Quick answers
- RxCUI (RxNorm): 692783
Why two NDCs?
The FDA registers this code as 68071-3904-4 — a 5-4-1 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 package segment → 68071-3904-04. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
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.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
📗 Our plain-language guide HelloPharmacist
- It temporarily relieves symptoms of hay fever and other upper respiratory allergies. That means runny nose, sneezing, itchy, watery eyes, and an itchy nose or throat.
- It is taken by mouth, generally once a day. Follow the directions on your specific product. Chewable tablets should be chewed or crushed completely, and liquids should be measured...
- No. Do not take more than directed. Taking more than directed may cause drowsiness. If you think you took too much, get medical help or call Poison Control right away.
- Can I take extra if my allergies are bad?
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about Loratadine?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 2, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 68071-3904-04 You're viewing this Main listing | 1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE | 2025-10-10 | — | Active |
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/5mLthis 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/5mL 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2020
On the market since
Aug 2020
📍
2026
Currently FDA-listed
6 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.
- FDA Orange Book · refreshed Sep 3, 2026
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.
Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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.
Manufacturer & labeler
LabelerNuCare Pharmaceuticals,Inc.
Application holderL PERRIGO CO
FDA applicationANDA075728 (ANDA)
Labeler code68071
First marketedAug 2020
Product typeHuman Otc Drug
Portfolio1,015 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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
📄 Do Not Use
📄 Ask a Doctor Before Use If
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
🤰 If Pregnant or Breast-Feeding
📄 Keep Out of Reach of Children
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 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
📦 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
📄 Do Not Use ▾
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 ▾
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 ▾
When using this product do not take more than directed. Taking more than directed may cause drowsiness.
📄 Stop Use and Ask a Doctor If ▾
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 pregnant or breast feeding, ask a health professional before use.
📄 Keep Out of Reach of Children ▾
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).
📄 Questions or Comments ▾
Questions or comments? 1-800-719-9260
📄 Package Label / Principal Display Panel ▾
Package/Label Principal Display Panel pdp
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 ↗
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 Good Sense childrens allergy relief (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 36%
Female · 64%
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.
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 | — Not published for this NDC No photo available yet for this listing. |
| 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.
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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 NuCare Pharmaceuticals,Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
NuCare Pharmaceuticals,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.
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.