Menthol Cough Drop 5.4 mg Lozenge, 80-count — NDC 37808-032-80 (Billing 37808-0032-80)
by HEB · 80 LOZENGE in 1 BAG
This is a package of 80 lozenges of Menthol Cough Drop 5.4 mg Lozenge from HEB, no longer marketed (first marketed May 2013), no longer in the FDA NDC Directory.
NDC 37808-0032-80
🏷️ FDA NDC (as labeled)
37808-032-80
billing pads the product segment with a zero
This package
Contains80-count
Pack sizes2 compare ↓
🗂️ 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 →
⚠️
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 ↗
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Jan 2024. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
37808-032-80
Product NDC
37808-032
11-digit billing NDC
37808003280
RxCUI
485287
UNII
L7T10EIP3A
Application #
M012
SPL Set ID
39178eb7-ada9-30bf-e054-00144ff88e88
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Discontinued by firm (certified through Jan 2024)
Marketing start
2013-05-15
Route
ORAL
Dosage form
LOZENGE
Substance
MENTHOL
Quick answers
- RxCUI (RxNorm): 485287
Why two NDCs?
The FDA registers this code as 37808-032-80 — 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 → 37808-0032-80. 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
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.
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about Menthol?
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 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.
Try another pack size:
30 lozenges
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 3, 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 |
|---|---|---|---|---|
| 37808-0032-30 37808-032-30 Main listing | 30 LOZENGE in 1 BAG | 2013-05-15 | — | Active |
| 37808-0032-80 You're viewing this | 80 LOZENGE in 1 BAG | 2013-05-15 | — | Discontinued by firm |
You're viewing the largest of 2 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
This is a 80-count package — 80 lozenge in 1 bag.
How does this package differ from NDC 37808-0032-30?
Both are Menthol Cough Drop 5.4 mg Lozenge — the drug itself is identical. This page's package is the 80-count one, while NDC 37808-0032-30 is the 30 lozenges package.
What NDC number is used to bill for this package of Menthol Cough Drop 5.4 mg Lozenge?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price 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 mgthis 37808-0032-80 | HEB | 80 lozenges | — | — | Discontinued | — |
| 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 mg 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2013
On the market since
May 2013
📍
2026
Currently FDA-listed
13 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.
- 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
LabelerHEB
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code37808
First marketedMay 2013
Product typeHuman Otc Drug
Portfolio89 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
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Ask a Doctor Before Use If
📄 Stop Use and Ask a Doctor If
🤰 If Pregnant or Breast-Feeding
📄 Keep Out of Reach of Children
📄 Other Information
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses temporarily relieves: cough as may occur with a cold occasional minor irritation and sore throat
⏱️ Dosage and Administration ▾
Directions adults and children 5 years and over - dissolve 1 lozenge slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor. children under 5 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, swelling, nausea, or vomiting, consut a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.
🧪 Active Ingredient ▾
Active Ingredient (in each drop) Menthol 5.4 mg
🧪 Inactive Ingredients ▾
Inactive ingredients: Corn starch, corn syrup, eucalyptus oil, FD&C blue no. 1, FD&C red no. 40, glycerin, gum arabic, medium chain triglycerides, natural flavors, potassium sorbate, soybean oil, sucrose and water.
🎯 Purpose ▾
Purpose Cough Suppressant / Oral anesthetic
📄 Ask a Doctor Before Use If ▾
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 (mucas)
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask doctor if cough persists for more than 7 days, tends to recur, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. sore throat is severe, or irritation, pain or redness lasts or worsens sore mouth does not improve in 7 days
🤰 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
📄 Other Information ▾
Other information 10 calories per drop
📄 Questions or Comments ▾
Questions? Or to report an adverse event call 1-800-245-2898 . Monday - Friday, 9AM to 4PM EST
📄 Package Label / Principal Display Panel ▾
HEB Menthol 30ct Cough Drops
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 Menthol Cough Drop (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.
About this NDC listing & data coverage
Over-the-counter (OTC) product
No longer marketed (per FDA listing data)
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | — Not published for this NDC No photo available yet for this listing. |
| Inactive ingredients (structured) | — 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
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 30 lozenges (37808-0032-30). 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?
HEB 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.