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Honey Lemon Cough Drop Menthol 7.5 mg Lozenge, 200-count — NDC 37808-0060-00 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Honey Lemon Cough Drop Menthol 7.5 mg Lozenge, 200-count — NDC 37808-060-00 (Billing 37808-0060-00)

by HEB · 200 LOZENGE in 1 BAG

This is a package of 200 lozenges of Honey Lemon Cough Drop Menthol 7.5 mg Lozenge from HEB, no longer marketed (first marketed May 2013), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 3 package sizes.

NDC 37808-0060-00
🏷️ FDA NDC (as labeled) 37808-060-00 billing pads the product segment with a zero
This package
Contains200-count Pack sizes3 compare ↓
Main listing for product 37808-060 · Also comes in: 30 lozenges 37808-060-30 80 lozenges 37808-060-80
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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 ↗
⚠️
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 Dec 2023. 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) 37808-060-00
Product NDC 37808-060
11-digit billing NDC 37808006000
RxCUI 1250189
UNII L7T10EIP3A
UPC 0041220176885
Application # M012
SPL Set ID 3a30a427-6ab4-24ae-e054-00144ff88e88
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Dec 2023)
Marketing start 2013-05-15
Route ORAL
Dosage form LOZENGE
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 1250189
Why two NDCs? The FDA registers this code as 37808-060-00 — 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 → 37808-0060-00. 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.
Try another pack size: 30 lozenges 80 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
37808-0060-30 37808-060-30 30 LOZENGE in 1 BAG 2013-05-15 — Active
37808-0060-80 37808-060-80 80 LOZENGE in 1 BAG 2013-05-15 — Discontinued by firm
37808-0060-00 You're viewing this Main listing 200 LOZENGE in 1 BAG 2013-05-15 — Discontinued by firm

You're viewing the largest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 200-count package — 200 lozenge in 1 bag.
How does this package differ from NDC 37808-0060-30?
Both are Honey Lemon Cough Drop Menthol 7.5 mg Lozenge — the drug itself is identical. This page's package is the 200-count one, while NDC 37808-0060-30 is the 30 lozenges package.
What NDC number is used to bill for this package of Honey Lemon Cough Drop Menthol 7.5 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

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 mgthis 37808-0060-00 HEB 200 lozenges — — Discontinued —
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/7.5mg 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 —
Amazon Basics Honey Lemon Cough Drops 30ct 7.5 mg 72288-0238-30 Amazon 30 lozenges — — FDA listed —
MGC Health Cough Drops Honey Lemon Flavor 7.5 mg 83173-0101-30 Medical 30 lozenges — — FDA listed —
Sanatos 7.5 mg 55758-0519-30 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

🏛️
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.

What it looks like

Color yellow
ShapeOval
ImprintB
Size17 mm
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 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.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesInactive ingredients: Beta carotene (color), corn starch, corn syrup, eucalyptus oil, glycerin, honey, medium chain triglycerides, natural and artificial flavors, soybean oil, sucrose and 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

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 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 16 words ▾

Uses temporarily relieves: cough as may occur with a cold occasional minor irritation and sore throat

⏱️ Dosage and Administration 35 words ▾

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 52 words ▾

Warngings 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, consult a docotr promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.

🧪 Active Ingredient 8 words ▾

Acitve ingredient (in each drop) Menthol 7.5 mg

🧪 Inactive Ingredients 25 words ▾

Inactive ingredients: Beta carotene (color), corn starch, corn syrup, eucalyptus oil, glycerin, honey, medium chain triglycerides, natural and artificial flavors, soybean oil, sucrose and water.

🎯 Purpose 6 words ▾

Purpose Cough suppressant / Oral anesthetic

📄 Ask a Doctor Before Use If 26 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)

📄 Stop Use and Ask a Doctor If 53 words ▾

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 10 words ▾

If pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Other Information 6 words ▾

Other information 10 calories per drop

📄 Questions or Comments 17 words ▾

Questions? Or to report an adverse event call 1-800-245-2898 . Monday - Friday, 9AM to 4PM EST.

📄 Package Label / Principal Display Panel 6 words ▾

HEB Honey Lemon 30ct Cough Drops

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 ✓ 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.
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 2 other package presentations of this same product, including 30 lozenges (37808-0060-30), 80 lozenges (37808-0060-80). 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.
← 37808-0058-36 · HEB 37808-0062-18 · HEB →
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.