MEDIQUE Medikoff Drops MENTHOL 7.6 mg Lozenge, 75-count
by Unifirst First Aid Corporation · 75 LOZENGE in 1 BOX (47682-050-22)
NDC 47682-0050-22
🏷️ FDA NDC (as labeled)
47682-050-22
billing pads the product segment with a zero
This package
Contains75-count
Pack sizes5 compare ↓
Also comes in:
6 lozenges 47682-0050-69
24 lozenges 47682-0050-64
600 lozenges 47682-0050-60
601 lozenges 47682-0050-66
OTC
On market
Non-controlled
🗂️ 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 →
⚠️
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
FDA NDC (as labeled)
47682-050-22
Product NDC
47682-050
11-digit billing NDC
47682005022
NCPDP billing unit
EA — each (per item)
RxCUI
359751
UNII
L7T10EIP3A
Application #
M012
SPL Set ID
0d6b4443-16a1-4851-bb03-d7407167551d
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2008-12-30
Route
ORAL
Dosage form
LOZENGE
Substance
MENTHOL
GPI-14
88200039004717
GPI class
Medikoff Drops
GCN Seq No
062487
GCN
98263
HICL code
019919
Ingredient (HICL)
Eucalyptus Oil/Menthol
HIC1 code
B
Therapeutic class — broad (HIC1)
Respiratory System
HIC2 code
B3
Therapeutic class — intermediate (HIC2)
Drugs Affecting Primarily The Trachea And Bronchi
HIC3 code
B3K
Therapeutic class — specific (HIC3)
Cough And/Or Cold Preparations
AHFS code
52:92.00.00
AHFS class
Eent Drugs, Miscellaneous
FDB label name
MEDIKOFF DROPS
FDB brand name
Medikoff
Legend status
O — Over-the-counter (OTC) drug or device
Why two NDCs?
The FDA registers this code as 47682-050-22 — 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 → 47682-0050-22. 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
LabelerUnifirst First Aid Corporation
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code47682
First marketedDec 2008
Product typeHuman Otc Drug
Portfolio179 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 MEDIKOFF DROPS Ingredient Eucalyptus Oil/Menthol
📗 Our plain-language guide HelloPharmacist
- Menthol is found in a lot of over-the-counter topical products — creams, gels, patches, sprays, and powders. Depending on the product, it's used to temporarily ease minor muscle an...
- Start with clean, dry skin — free of lotions or creams — before applying the patch. Peel the backing off and press the sticky side firmly to the sore area. Most menthol patches sho...
- Yes, a mild burning or tingling feeling right after applying a menthol product is common and usually settles down within a few days of regular use. What's not normal is severe burn...
- Is that burning sensation after I apply it normal?
Patient education
Supplement & herbal interactions
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
💬 Questions about MENTHOL?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
red
ShapeOval
ImprintP
Size22 mm
ScoringNot scored
FlavorCherry
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 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 WZB9127XOA
A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
-
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.
4 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesInactive ingredients cherry flavor, corn syrup, eucalyptus oil, FD&C red #40, sucrose
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 each | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| McKesson Cough Supressant 7.6 mg 68599-0500-03 | McKesson | 300 lozenges | $0.045 | — | Availability likely | — |
| Sugar Free Cough Drops Honey Lemon 7.6 mg 70000-0642-01 | Cardinal | 25 pastilles | $0.045 | — | Availability likely | — |
| Foster and Thrive SF Honey Lemon Cough Drops 7.6 mg 70677-1296-01 | McKesson | 80 lozenges | $0.045 | — | Availability likely | — |
| SF Honey Lemon Cough Drop 7.6 mg 00363-1077-25 | Walgreen | 25 lozenges | — | — | FDA listed | — |
| Sugar Free Honey Lemon Cough Drops 7.6 mg 00363-1094-50 | Walgreen | 150 lozenges | — | — | FDA listed | — |
| Physicians Care Cough and Sore Throat 7.6 mg 00924-0150-01 | Acme | 50 lozenges | — | — | FDA listed | — |
| Halls Sugar Free Honey Lemon 7.6 mg 12546-0642-25 | Mondelez | 25 lozenges | — | — | FDA listed | — |
| SF Honey Lemon Cough Drops 7.6 mg 30142-0034-25 | The | 25 lozenges | — | — | FDA listed | — |
| sugar free honey lemon cough drops 7.6 mg 36800-0822-25 | Topco | 25 lozenges | — | — | FDA listed | — |
| HEB SF Honey Lemon Cough Drops 7.6 mg 37808-0483-40 | HEB | 140 lozenges | — | — | FDA listed | — |
| sugar free honey lemon cough drops 7.6 mg 41250-0171-25 | Meijer | 25 lozenges | — | — | FDA listed | — |
| Sugar Free Honey Lemon Cough Drops 7.6 mg 41520-0045-25 | American | 25 lozenges | — | — | FDA listed | — |
| Green Guard Cough Drop Relief 7.6 mg 47682-0018-25 | Unifirst | 125 lozenges | — | — | FDA listed | — |
| MEDIQUE Medikoff Drops 7.6 mgthis 47682-0050-22 | Unifirst | 75 lozenges | — | — | FDA listed | — |
| MEDI-FIRST Cherry Cough Drops 7.6 mg 47682-0815-25 | Unifirst | 125 lozenges | — | — | FDA listed | — |
| Medi First Plus Cherry Cough Drops 7.6 mg 47682-0915-25 | Unifirst | 125 lozenges | — | — | FDA listed | — |
| Sugar Free Honey Lemon Cough Drops 7.6 mg 49035-0097-40 | Walmart | 140 lozenges | — | — | FDA listed | — |
| Unishield Cherry Cough 7.6 mg 49314-0505-05 | Unishield | 50 lozenges | — | — | FDA listed | — |
| Therastat, Cherry 7.6 mg 50332-0157-04 | HART | 50 lozenges | — | — | FDA listed | — |
| Good Sense SF Honey Lemon Cough Drops 7.6 mg 50804-0028-25 | Geiss, | 25 lozenges | — | — | FDA listed | — |
| Sugar Free Cough Drops 7.6 mg 51316-0848-01 | CVS | 36 pastilles | — | — | FDA listed | — |
| Menthol Cough Drops Honey Lemon Flavor 7.6 mg 51316-0988-01 | CVS | 140 pastilles | — | — | FDA listed | — |
| Sugar Free Honey Lemon Cough Drops 7.6 mg 52642-0045-25 | Bestco | 25 lozenges | — | — | FDA listed | — |
| Exchange Select Cough Drops Honey Lemon Sugar-Free 7.6 mg 55301-0583-25 | Army | 25 lozenges | — | — | FDA listed | — |
| Family Wellness SF Honey Lemon Cough Drops 7.6 mg 55319-0080-25 | Family | 25 lozenges | — | — | FDA listed | — |
| sugar free honey lemon cough drops 7.6 mg 59779-0697-36 | CVS | 36 lozenges | — | — | FDA listed | — |
| CVS SF Honey Lemon Cough Drops 7.6 mg 69842-0594-40 | CVS | 140 lozenges | — | — | FDA listed | — |
| Redicare Cough Drops Cherry Flavored 7.6 mg/100mg 71105-0930-01 | Redicare | 50 packets | — | — | FDA listed | — |
| Harris Teeter SF Honey Lemon Cough Drops 7.6 mg 72036-0084-25 | Harris | 25 lozenges | — | — | FDA listed | — |
| Basic Care SF Honey Lemon Cough Drops 7.6 mg 72288-0236-40 | Amazon.com | 140 lozenges | — | — | FDA listed | — |
| Honey Lemon Cough Drops 7.6 mg 72628-0102-01 | Boston | 36 pastilles | — | — | FDA listed | — |
| Honey Lemon Cough Drops 7.6 mg 72628-0103-01 | Boston | 150 pastilles | — | — | FDA listed | — |
| Honey Lemon Cough Drops 7.6 mg 72628-0109-01 | Boston | 25 pastilles | — | — | FDA listed | — |
| Thompson Cherry Cough Drops 7.6 mg 73408-0815-50 | Thompson | 50 lozenges | — | — | FDA listed | — |
| Cherry Cough Drops 50Ct 7.6 mg 73598-1202-01 | JHK | 50 lozenges | — | — | FDA listed | — |
| Cherry Cough Drops 100Ct 7.6 mg 73598-1204-01 | JHK | 100 lozenges | — | — | FDA listed | — |
| Sugar Free Cough Drops 7.6 mg 76162-0028-01 | Topco | 25 pastilles | — | — | FDA listed | — |
| MGC Health 7.6 mg 83173-0115-25 | Medical | 25 lozenges | — | — | FDA listed | — |
| Quality Choice Honey Lemon Sugar Free Cough Drops 7.6 mg 83324-0288-25 | Chain | 25 lozenges | — | — | FDA listed | — |
| Cough Drops 7.6 mg 83455-0200-01 | United | 25 pastilles | — | — | FDA listed | — |
| MGC Health 7.6 mg 83698-0125-25 | Xiamen | 25 lozenges | — | — | FDA listed | — |
| Exchange Select Cough Drops Honey Lemon Sugar-Free 7.6 mg 83698-0583-25 | Xiamen | 25 lozenges | — | — | FDA listed | — |
| Quality Choice 7.6 mg 83698-0616-25 | Xiamen | 25 lozenges | — | — | FDA listed | — |
| SF Honey Lemon Cough Drops 7.6 mg 41250-0172-50 | Meijer | 150 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
🏛️
2008
On the market since
Dec 2008
📍
2026
Currently FDA-listed
18 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.
🔬 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 MEDIQUE Medikoff Drops (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 38%
Female · 62%
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 |
|---|---|---|---|
| 47682-0050-22 You're viewing this | 75 LOZENGE in 1 BOX (47682-050-22) | 2008-12-30 | Active |
| 47682-0050-60 | 600 LOZENGE in 1 BOX (47682-050-60) | 2008-12-30 | Active |
| 47682-0050-64 | 24 LOZENGE in 1 BOX (47682-050-64) | 2008-12-30 | Active |
| 47682-0050-66 | 601 LOZENGE in 1 BOX (47682-050-66) | 2008-12-30 | Active |
| 47682-0050-69 | 6 LOZENGE in 1 BOX (47682-050-69) | 2008-12-30 | Active |
You're viewing one of 5 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 47682-0050-22?
NDC 47682-0050-22 is a 75-count package — 75 lozenge in 1 box.
What is the difference between NDC 47682-0050-22 and NDC 47682-0050-69?
Both are MEDIQUE Medikoff Drops MENTHOL 7.6 mg Lozenge — the drug itself is identical. NDC 47682-0050-22 is the 75-count package, while NDC 47682-0050-69 is the 6 lozenges package.
What NDC number is used to bill for this package of MEDIQUE Medikoff Drops MENTHOL 7.6 mg Lozenge?
Bill NDC 47682-0050-22 — the 11-digit billing format is 47682005022. 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
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 FDA registers it as 47682-050-22, 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: 47682-0050-22, written without dashes as 47682005022. 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 47682-0050-22, the first segment (47682) is the labeler code FDA assigned to Unifirst First Aid Corporation; the middle segment (0050) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (22) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Unifirst First Aid Corporation. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 4 other package presentations of this same product, including 6 lozenges (47682-0050-69), 24 lozenges (47682-0050-64), 600 lozenges (47682-0050-60). 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?
Unifirst First Aid Corporation 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
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses Temporarily relieves ■ cough as may occur with a cold or inhaled irritants ■ occasional minor irritation and sore throat
⏱️ Dosage and Administration ▾
Directions do not use more than directed Adults and children: (12 years and older) Allow 1 drop to dissolve slowly in the mouth. May be repeated every 2 hours as necessary or as directed by a doctor. Children under 12 years: Ask a doctor
⚠️ Warnings ▾
Warnings Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly. These symptoms may be serious. Ask a doctor before use if you have ■ persistent or chronic cough such as occurs with smoking, asthma, or emphysema ■ cough accompanied by excessive phlegm (mucus) Stop use and ask a doctor if ■ cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache.
These could be signs of a serious condition. ■ sore mouth does not improve in 7 days ■ irritation, pain, or redness persists or worsens
🧪 Active Ingredient ▾
Active ingredient (in each drop) Menthol 7.6 mg
🧪 Inactive Ingredients ▾
Inactive ingredients cherry flavor, corn syrup, eucalyptus oil, FD&C red #40, sucrose
🎯 Purpose ▾
Purpose Antitussive (cough suppressant)/oral anesthetic
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.