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Exchange Select Cough Drops Menthol Sugar Free 5.4 mg Lozenge, 25-count — NDC 55301-0584-25 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Exchange Select Cough Drops Menthol Sugar Free 5.4 mg Lozenge, 25-count — NDC 55301-584-25 (Billing 55301-0584-25)

by Army & Air Force Exchange Service · 25 LOZENGE in 1 BAG

This is a package of 25 lozenges of Exchange Select Cough Drops Menthol Sugar Free 5.4 mg Lozenge from Army & Air Force Exchange Service, marketed since Jun 2025 and currently FDA-listed. It is this product's only package size.

NDC 55301-0584-25
🏷️ FDA NDC (as labeled) 55301-584-25 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

⚠️
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) 55301-584-25
Product NDC 55301-584
11-digit billing NDC 55301058425
RxCUI 485287
UNII L7T10EIP3A
Application # M012
SPL Set ID 3805ef07-247d-0df7-e063-6394a90ac45b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-06-20
Route ORAL
Dosage form LOZENGE
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 485287
Why two NDCs? The FDA registers this code as 55301-584-25 — 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 → 55301-0584-25. 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
55301-0584-25 You're viewing this Main listing 25 LOZENGE in 1 BAG 2025-06-20 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Cough Drops Menthol 5.4 mg 70000-0638-01 Cardinal 30 pastilles $0.034 — Availability likely —
Menthol Cough Drop 5.4 mg 00363-1070-30 Walgreens 30 lozenges — — FDA listed —
Walgreens Menthol Cough Drops 5.4 mg 00363-9957-40 Walgreens 40 lozenges — — FDA listed —
Halls MENTHO-LYPTUS 5.4 mg 12546-0112-14 Mondelez 14 lozenges — — Discontinued —
HALLS Mentholyptus 5.4 mg 12546-0116-30 Mondelez 30 lozenges — — FDA listed —
Menthol Cough Drop 5.4 mg 21130-0265-30 Safeway 30 lozenges — — FDA listed —
Menthol cough drop 5.4 mg 30142-0031-30 The 30 lozenges — — FDA listed —
menthol cough drops 5.4 mg 36800-0814-30 Topco 30 lozenges — — FDA listed —
Menthol Cough Drop 5.4 mg 37808-0032-30 HEB 30 lozenges — — FDA listed —
HEB Menthol Cough Drops 5.4 mg 37808-0475-60 HEB 160 lozenges — — FDA listed —
Menthol Cough Drops 5.4 mg 41250-0082-00 Meijer 200 lozenges — — FDA listed —
menthol cough drops 5.4 mg 41250-0149-04 Meijer 30 lozenges — — FDA listed —
menthol cough drops 5.4 mg 41520-0009-30 American 30 lozenges — — FDA listed —
HyVee Cough Drops Menthol 5.4 mg 42507-0905-30 HY-VEE, 30 lozenges — — FDA listed —
GoodSense Menthol Cough Drops 5.4 mg 50804-0013-30 Geiss, 30 lozenges — — FDA listed —
Cough Drops 5.4 mg 50804-0592-01 Perrigo 30 pastilles — — FDA listed —
Menthol Cough Drops 5.4 mg 52642-0042-30 Bestco 30 lozenges — — FDA listed —
Best Health Menthol Cough Drops 5.4 mg 52642-0055-80 Bestco 80 lozenges — — FDA listed —
Discount Drug Mart 5.4 mg 53943-0102-30 DISCOUNT 30 lozenges — — FDA listed —
Menthol Flavor Cough Drop 5.4 mg 55301-0581-30 Army 30 lozenges — — FDA listed —
Exchange Select Cough Drops Menthol Sugar Free 5.4 mgthis 55301-0584-25 Army 25 lozenges — — FDA listed —
Menthol cough drops 5.4 mg 55319-0006-30 Family 30 lozenges — — FDA listed —
Cough Drops 5.4 mg 59450-0713-01 The 30 pastilles — — FDA listed —
Cough Drops 5.4 mg 59450-0714-01 The 200 pastilles — — FDA listed —
menthol cough drops 5.4 mg 67091-0300-80 Winco 80 lozenges — — FDA listed —
Premier Value 5.4 mg 68016-0885-30 Pharmacy 4 lozenges — — FDA listed —
CVS Menthol Cough Drops 5.4 mg 69842-0536-60 CVS 160 lozenges — — FDA listed —
Freegells Cough Drops Menthol Eucalyptus 5.4 mg 71165-0012-00 Riclan 30 lozenges — — FDA listed —
Harris Teeter Menthol Cough Drops 5.4 mg 72036-0085-30 Harris 30 lozenges — — FDA listed —
Menthol Cough Drops 5.4 mg 72628-0118-01 BOSTON 30 pastilles — — FDA listed —
Cough Drops Dollar General Menthol 30ct 5.4 mg 75712-0017-01 Dollar 270 lozenges — — FDA listed —
Cough Drops Dollar General Menthol 80ct 5.4 mg 75712-0021-01 Dollar 480 lozenges — — FDA listed —
Cough Drops Dollar General Menthol 160ct 5.4 mg 75712-0023-01 Dollar 640 lozenges — — FDA listed —
Cough Drops 5.4 mg 76162-0011-01 Topco 30 pastilles — — FDA listed —
Equate Menthol Cough Drops 5.4 mg 79903-0253-30 Walmart 30 lozenges — — FDA listed —
Freegells Cough Drops Menthol 80ct 5.4 mg 83002-0004-01 R.L. 480 lozenges — — FDA listed —
Freegells Cough Drops Menthol 30ct 5.4 mg 83002-0005-01 R.L. 270 lozenges — — FDA listed —
MGC Cough Drops 5.4 mg 83173-0109-30 Medical 30 lozenges — — FDA listed —
MGC Health 5.4 mg 83173-0113-25 Medical 25 lozenges — — FDA listed —
Quality Choice Menthol Cough Drops 5.4 mg 83324-0265-30 Chain 30 lozenges — — FDA listed —
Cough Drops 5.4 mg 83455-0206-01 United 30 pastilles — — FDA listed —
Discount Drug Mart 5.4 mg 83698-0102-30 Xiamen 30 lozenges — — FDA listed —
MENTHOL COUGH SUPPRESSANT ORAL ANESTHETIC Cough Drops 5.4 mg 83698-0110-30 Xiamen 30 lozenges — — FDA listed —
MGC Health 5.4 mg 83698-0113-25 Xiamen 25 lozenges — — FDA listed —
Menthol Flavor Cough Drop 5.4 mg 83698-0581-30 Xiamen 30 lozenges — — FDA listed —
Exchange Select Cough Drops Menthol Sugar Free 5.4 mg 83698-0584-25 Xiamen 25 lozenges — — FDA listed —
Quality Choice 5.4 mg 83698-0675-30 Xiamen 30 lozenges — — FDA listed —
Premier Value 5.4 mg 83698-0885-30 Xiamen 4 lozenges — — FDA listed —
HyVee Cough Drops Menthol 5.4 mg 83698-0901-30 Xiamen 30 lozenges — — FDA listed —
Sanatos 5.4 mg 55758-0518-30 Pharmadel 900 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

🏛️
2025
On the market since
Jun 2025
📍
2026
Currently FDA-listed
1 year 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 blue
ShapeOval
Size21 mm
FlavorMenthol
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 5C5403N26O
    Acacia is a natural gum derived from acacia tree sap. It serves as a binder, thickener, and emulsifier to help hold ingredients together, improve texture, and stabilize the medicine.
  • UNII 23OV73Q5G9
    Acesulfame potassium is an artificial sweetener that tastes about 200 times sweeter than sugar. It's added to medicines to improve taste without adding calories or affecting blood sugar.
  • 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 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 H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • 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 S870P55O2W
    Isomalt is a sugar alcohol made from sugar that's used as a sweetener and bulking agent in medicines. It helps give tablets and powders the right texture and sweetness while having minimal calories.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • 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 89NA02M4RX
    Pectin is a natural fiber extracted from fruit and plants. It's used in medicines as a thickener, binder, and gelling agent to create the right texture and help the product hold together.
  • UNII EE90ONI6FF
    Potassium citrate is a salt derived from citric acid and potassium. In medicines, it acts as a buffer to adjust and maintain the pH balance of the product, helping keep it stable and palatable.
  • 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 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.

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

The official label also statesacacia, acesulfame potassium, citric acid, corn starch, eucalyptus oil, FD&C blue 1, FD&C red 40, isomalt, maltitol, menthol flavor, pectin, potassium citrate, soy lecithin, sucralose, water

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.

Manufacturer & labeler

LabelerArmy & Air Force Exchange Service
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code55301
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio44 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 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 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 17 words ▾

Use temporary relieves: cough due to a cold occasional minor irritation, pain, sore mouth, and sore throat

⏱️ Dosage and Administration 32 words ▾

Directions Adults and children 2 years and over: dissolve lozenge slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor. Children under 2 years: ask a doctor.

⚠️ Warnings 32 words ▾

Warnings Sore throat warning: If sore throat is severe, persists for more than 2 days, or is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly.

📦 Storage and Handling 27 words ▾

Other information Store at room temperature Keep away from excessive heat or sunlight Do not use if primary bag seal has been torn or broken Contains: SOY

🧪 Active Ingredient 5 words ▾

Active Ingredient(s) Menthol 5.4 mg

🧪 Inactive Ingredients 28 words ▾

Inactive ingredients acacia, acesulfame potassium, citric acid, corn starch, eucalyptus oil, FD&C blue 1, FD&C red 40, isomalt, maltitol, menthol flavor, pectin, potassium citrate, soy lecithin, sucralose, water

🎯 Purpose 6 words ▾

Purpose Purposes cough suppressant, oral anesthetic

📄 Ask a Doctor Before Use If 28 words ▾

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).

📄 When Using This Product 9 words ▾

When using this product: Do not exceed recommended dosage.

📄 Stop Use and Ask a Doctor If 53 words ▾

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 (a persistent cough may be a sign of a serious condition) sore mouth symptoms don’t improve in 7 days irritation, pain, or redness persists or worsens

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Questions or Comments 9 words ▾

Call +8009352362 Available Monday–Friday, 9 AM–5 PM Eastern Time

📄 Package Label / Principal Display Panel 9 words ▾

Package Label - Principal Display Panel Menthol Cough Drop

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 Exchange Select Cough Drops Menthol Sugar Free (this brand).

Top reported reactions

Dyspnoea85
Fatigue84
Pain81
Pruritus78
Dizziness67
Headache67
Cough65

Age at onset

Infant1
Child1
Adolescent1
Adult95
Elderly90

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 66
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 Army & Air Force Exchange Service. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Army & Air Force Exchange Service 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.
← 55301-0583-25 · Army 55301-0585-60 · Army →
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.