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Cough Drops Honey Lemon with Sugar Menthol 7.5 mg/7.5mg Tablet, 96000 mg — NDC 71141-0110-32 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Cough Drops Honey Lemon with Sugar Menthol 7.5 mg/7.5mg Tablet, 96000 mg — NDC 71141-110-32 (Billing 71141-0110-32)

by Lidl US LLC · 96000 mg in 1 BAG

This is a package of 96,000 mg of Cough Drops Honey Lemon with Sugar Menthol 7.5 mg/7.5mg Tablet from Lidl US LLC, marketed since May 2017 and currently FDA-listed. It is this product's only package size.

NDC 71141-0110-32
🏷️ FDA NDC (as labeled) 71141-110-32 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ 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 →

This page is curated, coded, and maintained by

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

NDC database record

One package, one record: these facts belong to NDC 71141-110-32 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
71141 labeler · 110 product · 32 package
Package marketed since
May 1, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7114111032 4
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Menthol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 20, 2026 — This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality. (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.) · FDA recall D-0458-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 71141-110-32
Product NDC 71141-110
11-digit billing NDC 71141011032
RxCUI 476973, 1250189
UNII L7T10EIP3A
Application # M012
SPL Set ID 4ad9398f-7488-6eaf-e054-00144ff8d46c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-05-01
Route ORAL
Dosage form TABLET
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 476973
Why two NDCs? The FDA registers this code as 71141-110-32 — 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 → 71141-0110-32. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • Mostly for temporary relief of minor aches and pains in muscles and joints, like those from arthritis, backache, strains, sprains and bruises. Some products are for other things, s...
  • It depends on the product. Many creams, gels and patches are limited to about 3 to 4 times a day, and patches also have a time limit, often 8 hours. Follow your product label and a...
  • A brief burning feeling can happen when you first apply it and usually fades in several days. But if you get severe burning pain, swelling or blistering, stop using it and call you...
  • No. Don't use menthol products with a heating pad, and avoid local heat or direct sunlight on the area. Rare cases of serious burns have been reported.
📖 Read our full Menthol 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.

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.
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
71141-0110-32 You're viewing this Main listing 96000 mg in 1 BAG 2017-05-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Cough Drops Menthol Honey Lemon 7.5 mg 70000-0639-01 Cardinal 30 pastilles $0.034 — Availability likely —
Foster and Thrive Honey Lemon Cough Drops 7.5 mg 70677-1297-01 McKesson 80 lozenges $0.034 — Availability likely —
Honey Lemon Cough Drop 7.5 mg 00363-1072-30 Walgreens 30 lozenges — — FDA listed —
Honey Lemon Cough Drop 7.5 mg 00363-1087-00 Walgreen 200 lozenges — — FDA listed —
Walgreens Honey Lemon Cough Drops 7.5 mg 00363-9959-40 Walgreens 40 lozenges — — FDA listed —
Halls Honey Lemon 7.5 mg 12546-0110-00 Mondelez 250 lozenges — — FDA listed —
Signature Care Honey Lemon Cough Drops 7.5 mg 21130-0309-00 Safeway 200 lozenges — — FDA listed —
Honey Lemon Cough Drop 7.5 mg 30142-0028-80 The 80 lozenges — — FDA listed —
honey lemon cough drops 7.5 mg 36800-0816-00 Topco 200 lozenges — — Discontinued —
Honey Lemon Cough Drop 7.5 mg 37808-0060-30 HEB 30 lozenges — — FDA listed —
HEB Honey Lemon Cough Drops 7.5 mg 37808-0474-60 HEB 160 lozenges — — FDA listed —
honey lemon cough drops 7.5 mg 41250-0155-30 Meijer 30 lozenges — — FDA listed —
honey lemon cough drops 7.5 mg 41250-0156-00 Meijer 200 lozenges — — FDA listed —
Honey Lemon Cough Drops 7.5 mg 41415-0009-30 Publix 30 lozenges — — FDA listed —
honey lemon cough drops 7.5 mg 41520-0011-30 American 30 lozenges — — FDA listed —
HyVee Cough Drops Honey Lemon 7.5 mg 42507-0904-30 HY-VEE, 30 lozenges — — FDA listed —
Honey Lemon Flavor Cough Drops 7.5 mg 42681-0038-01 WHOLE 30 pastilles — — FDA listed —
Honey Lemon cough drops 7.5 mg 49035-0027-60 Walmart 160 lozenges — — FDA listed —
Good Sense Honey Lemon Cough Drops 7.5 mg 50804-0021-30 Geiss, 30 lozenges — — FDA listed —
Cough Drops 7.5 mg 50804-0593-01 Perrigo 30 pastilles — — FDA listed —
Menthol Cough Drops Honey Lemon Flavor 7.5 mg 51316-0987-01 CVS 140 pastilles — — FDA listed —
Honey Lemon Cough Drops 7.5 mg 52642-0044-30 Bestco 30 lozenges — — FDA listed —
Discount Drug Mart 7.5 mg 53943-0150-30 DISCOUNT 30 lozenges — — FDA listed —
Honey Lemon Flavor Cough Drop 7.5 mg 55301-0580-30 Army 30 lozenges — — FDA listed —
honey lemon cough drops 7.5 mg 55319-0008-30 Family 30 lozenges — — FDA listed —
Cough Drops 7.5 mg 59450-0715-01 The 30 pastilles — — FDA listed —
Cough Drops 7.5 mg 59450-0716-01 The 80 pastilles — — FDA listed —
Cough Drops 7.5 mg 59450-0717-01 The 200 pastilles — — FDA listed —
honey lemon cough drops 7.5 mg 67091-0302-30 Winco 30 lozenges — — FDA listed —
Premier Value 7.5 mg 68016-0884-30 Pharmacy 30 lozenges — — FDA listed —
CVS Honey Lemon Cough Drops 7.5 mg 69842-0534-60 CVS 160 lozenges — — FDA listed —
Cough Drops Honey Lemon with Sugar 7.5 mg/7.5mgthis 71141-0110-32 Lidl 96000 mg — — FDA listed —
Freegells Cough Drops Menthol Honey Lemon 7.5 mg 71165-0013-00 Riclan 30 lozenges — — FDA listed —
Harris Teeter Honey Lemon Cough Drops 7.5 mg 72036-0083-30 Harris 30 lozenges — — FDA listed —
Basic Care Honey Lemon Cough Drops 7.5 mg 72288-0232-60 Amazon.com 160 lozenges — — FDA listed —
Cough Drops Dollar General Honey Lemon 30ct 7.5 mg 75712-0015-01 Dollar 270 lozenges — — FDA listed —
Cough Drops Dollar General Honey Lemon 200ct 7.5 mg 75712-0020-01 Dollar 800 lozenges — — FDA listed —
Honey Lemon Menthol Cough Drops 7.5 mg 76162-0024-01 Topco 30 pastilles — — FDA listed —
Cough Drops 7.5 mg 76162-0025-01 Topco 80 pastilles — — FDA listed —
Cough Drops 7.5 mg 76162-0027-01 Topco 160 pastilles — — FDA listed —
Equate Honey Lemon Cough Drops 7.5 mg 79903-0192-30 WalMart 30 lozenges — — FDA listed —
Freegells Cough Drops Menthol Honey Lemon 30ct 7.5 mg 83002-0006-01 R.L. 270 lozenges — — FDA listed —
Freegells Cough Drops Menthol Honey Lemon 200ct 7.5 mg 83002-0007-01 R.L. 800 lozenges — — FDA listed —
Freegells Cough Drops Menthol Honey Lemon 80ct 7.5 mg 83002-0009-01 R.L. 480 lozenges — — FDA listed —
MGC Health 7.5 mg 83173-0114-30 Medical 30 lozenges — — FDA listed —
Quality Choice Honey Lemon Cough Drops 7.5 mg 83324-0279-30 Chain 30 lozenges — — FDA listed —
Cough Drops 7.5 mg 83455-0203-01 United 30 pastilles — — FDA listed —
MGC Health 7.5 mg 83698-0114-30 Xiamen 30 lozenges — — FDA listed —
Discount Drug Mart 7.5 mg 83698-0150-30 Xiamen 30 lozenges — — FDA listed —
Honey Lemon Flavor Cough Drop 7.5 mg 83698-0580-30 Xiamen 30 lozenges — — FDA listed —
Quality Choice 7.5 mg 83698-0617-30 Xiamen 30 lozenges — — FDA listed —
Premier Value 7.5 mg 83698-0884-30 Xiamen 30 lozenges — — FDA listed —
HyVee Cough Drops Honey Lemon 7.5 mg 83698-0903-30 Xiamen 30 lozenges — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
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

🏛️
2017
On the market since
May 2017
📍
2026
Currently FDA-listed
9 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

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.

What it looks like

Color red / white / yellow
ShapeOval
Size2 mm
ScoringNot scored
FlavorHoney
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 H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • UNII 7QWA1RIO01
    A synthetic form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the formulation from breaking down, helping the drug remain stable and effective during storage.
  • UNII 01YAE03M7J
    Beta carotene is a naturally occurring orange pigment found in plants. In medicines, it serves as a colorant to make tablets or capsules appear orange or yellow.
  • UNII K4K90ZQ89N
    A synthetic compound used as a solvent and preservative in liquid medications. It helps dissolve active ingredients and prevents microbial growth to maintain product stability.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII PQ6CK8PD0R
    Ascorbic acid, also known as vitamin C, is a white crystalline powder. It serves as an antioxidant to prevent degradation of other ingredients and may also function as a preservative in the formulation.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII 9G5L16BK6N
    A thick, sweet liquid made from corn starch. It acts as a sweetener, thickener, and binder in medicines, helping create the right texture and taste while holding ingredients together.
  • UNII 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • UNII Y9H1V576FH
    Honey is a natural sweetener made by bees from flower nectar. In medicines, it adds sweetness to improve taste and may help soothe throat irritation in lozenges or syrups.
  • UNII 33X04XA5AT
    Lactic acid is a naturally occurring organic acid derived from milk or plant sources. It lowers and maintains pH in formulations, helps preserve the product, and can enhance ingredient stability and absorption.
  • UNII AGN709ANTJ
    A natural liquid extracted from lemons, containing citric acid and water. It's used as a flavoring agent and acidifying ingredient to enhance taste and help maintain the medicine's pH balance.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
  • 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 C151H8M554
    A natural sugar derived from sugar cane or sugar beets. It's used as a sweetener, filler, and binder to improve taste, add bulk, and help hold tablet or capsule ingredients together.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII XHX3C3X673
    Triacetin is a clear, oily liquid made from glycerin and acetic acid. It works as a plasticizer and solvent in medicines, helping soften coatings and improve how liquids mix together in formulations.
  • 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.

20 inactive ingredients listed in the exact product block matched to this NDC.

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.

Manufacturer & labeler

LabelerLidl US LLC
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code71141
First marketedMay 2017
Product typeHuman Otc Drug
Portfolio16 products on file

More NDCs from Lidl US LLC labeler code 71141

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 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 20 words ▾

Cough drops Honey Lemon Honey Lemon Indication Use

Cough drops Menthol Menthol Indication and Usage

Cough Drops Cherry Cherry Indication

⏱️ Dosage and Administration 23 words ▾

Cough Drops Honey lemon Honey Lemon Dosage and Administration

Cough Drops Menthol Menthol Dosage and Administration

Cough Drops Cherry Cherry Dosage and Administration

⚠️ Warnings 18 words ▾

Cough drops Honey Lemon Honey Lemon warning Section

Cough drops Menthol Menthol Warning

Cough Drops Cherry Cherry warning

🧪 Active Ingredient 20 words ▾

Cough Drops Honey Lemon Honey Lemon Active Ingredients

Cough Drops Menthol Menthol Active Ingredient

Cough Drops Cherry Cherry Active Ingredient

🧪 Inactive Ingredients 20 words ▾

Cough Drops Honey lemon Honey Lemon Inactive Ingredients

Cough Drops Menthol Menthol Inactive Ingredient

Cough Drops Cherry Cherry Inactive Ingredient

🎯 Purpose 23 words ▾

Cough Drops Honey Lemon Purpose Cough Suppressant/ Oral Anesthetic Honey lemon Purpose

Cough drops Menthol menthol Purpose

OTC-Purpose Cough Drops Cherry Cherry Purpose

📄 Keep Out of Reach of Children 30 words ▾

Cough Drops Honey Lemon Honey Lemon Keep out of reach of children

Cough drops Menthol Menthol Keep out of reach of children

Cough Drops Cherry Cherry Keep out of reach

📄 Package Label / Principal Display Panel 196 words ▾

Cough Drops Honey Lemon Tray content: 4 Menthol bags 4 Cherry bags 4 Honey Lemon bags Honey Lemon bag Front and Backside Display Cough Drops Honey Lemon Honey Lemon Active Ingredients Cough Drops Honey Lemon Purpose Cough Suppressant/ Oral Anesthetic Honey lemon Purpose Cough drops Honey Lemon Honey Lemon Indication Use Cough drops Honey Lemon Honey Lemon warning Section Cough Drops Honey Lemon Honey Lemon Keep out of reach of children Cough Drops Honey lemon Honey Lemon Dosage and Administration Cough Drops Honey lemon Honey Lemon Inactive Ingredients

Cough Drops Menthol Bag Menthol Front and Backside tray menthol Cough Drops Menthol Menthol Active Ingredient Cough drops Menthol menthol Purpose Cough drops Menthol Menthol Indication and Usage Cough drops Menthol Menthol Warning Cough drops Menthol Menthol Keep out of reach of children Cough Drops Menthol Menthol Dosage and Administration Cough Drops Menthol Menthol Inactive Ingredient

Cough Drops Cherry Bag Cherry Front and Backside Tray Cough Drops Cherry Cherry Active Ingredient OTC-Purpose Cough Drops Cherry Cherry Purpose Cough Drops Cherry Cherry Indication Cough Drops Cherry Cherry warning Cough Drops Cherry Cherry Keep out of reach Cough Drops Cherry Cherry Dosage and Administration Cough Drops Cherry Cherry Inactive Ingredient

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 Cough Drops Honey Lemon with Sugar (this brand).

Top reported reactions

Dyspnoea85
Fatigue84
Pain81
Pruritus78
Dizziness67
Headache67
Cough65

Reporter sex

989 reports
Male · 38%
Female · 62%
Unknown · 0%

Serious outcomes

Hospitalization333
Death125
Life-threatening45
Disabling26
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 109 0
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 ✓ 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

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
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 Lidl US LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Lidl US 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.
← 71141-0022-02 · LIDL 71141-0111-32 · Lidl →
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.