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Honey Lemon Cough Drops Menthol 7.6 mg Pastille, 150-count — NDC 72628-0103-01 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 Drops Menthol 7.6 mg Pastille, 150-count — NDC 72628-103-01 (Billing 72628-0103-01)

by Boston Nutraceutical Production SL · 150 PASTILLE in 1 BAG

This is a package of 150 pastilles of Honey Lemon Cough Drops Menthol 7.6 mg Pastille from Boston Nutraceutical Production SL, marketed since Mar 2019 and currently FDA-listed. It is this product's only package size.

NDC 72628-0103-01
🏷️ FDA NDC (as labeled) 72628-103-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

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

NDC database record

One package, one record: these facts belong to NDC 72628-103-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
72628 labeler · 103 product · 01 package
Package marketed since
Mar 26, 2019
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7262810301 3
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Menthol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 20, 2026 — This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality. (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.) · FDA recall D-0458-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72628-103-01
Product NDC 72628-103
11-digit billing NDC 72628010301
RxCUI 359751
UNII L7T10EIP3A
Application # M012
SPL Set ID 856f0bd8-354b-a002-e053-2a91aa0a8022
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-03-26
Route ORAL
Dosage form PASTILLE
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 359751
Why two NDCs? The FDA registers this code as 72628-103-01 — 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 → 72628-0103-01. 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
72628-0103-01 You're viewing this Main listing 150 PASTILLE in 1 BAG 2019-03-26 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
McKesson Cough Supressant 7.6 mg 68599-0500-03 McKesson 300 lozenges $0.044 — Availability likely —
Sugar Free Cough Drops Honey Lemon 7.6 mg 70000-0642-01 Cardinal 25 pastilles $0.044 — Availability likely —
Foster and Thrive SF Honey Lemon Cough Drops 7.6 mg 70677-1296-01 McKesson 80 lozenges $0.044 — 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 mg 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 mgthis 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

🏛️
2019
On the market since
Mar 2019
📍
2026
Currently FDA-listed
7 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
ImprintNone
Size17 mm
FlavorLemon
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 XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • UNII Y9H1V576FH
    Honey is a natural sweetener made by bees from flower nectar. In medicines, it adds sweetness to improve taste and may help soothe throat irritation in lozenges or syrups.
  • UNII 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 I9GRO824LL
    Lemon oil is a natural fragrant extract from lemon peel. It's used in medicines as a flavoring agent to mask unpleasant tastes and improve how the medicine tastes to patients.
  • UNII 6U422Y08O2
    A natural sweetener derived from stevia plant leaves. It provides sweetness to the medicine with minimal calories and is used to improve taste, making the medication more palatable.
  • UNII 856YO1Z64F
    Turmeric is a natural spice derived from the turmeric plant root. It serves as a colorant in medicines, giving products a yellow or golden appearance, and may also provide mild flavoring.
  • 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.

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

The official label also statesCitric acid, eucalyptus oil, isomalt, stevia, flavor lemon oil, flavor honey extract, colorant turmeric, 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

LabelerBoston Nutraceutical Production SL
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code72628
First marketedMar 2019
Product typeHuman Otc Drug
Portfolio6 products on file

More NDCs from Boston Nutraceutical Production SL labeler code 72628

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 🆘 Overdosage 🧪 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 18 words ▾

Uses Temporarily relieves: cough as may occur with cold or inhaled irritants ocassional minor irritations and sore throat

⏱️ Dosage and Administration 37 words ▾

Directions Adults and children 5 years and over: allow 1 drop to dissolve slowly in mouth. May be repeated every two hours as necessary or as directed by a doctor. Children under 5 years: ask a doctor

⚠️ Warnings 52 words ▾

Warnings Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swealing, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptons may be serious.

🆘 Overdosage 16 words ▾

In case of accidental overdose, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 15 words ▾

Active Ingredient in each drop Purposes Menthol 7.6 mg Cough Suppressant Oral anesthetic Front label

🧪 Inactive Ingredients 17 words ▾

Citric acid, eucalyptus oil, isomalt, stevia, flavor lemon oil, flavor honey extract, colorant turmeric, water Back Label

🎯 Purpose 5 words ▾

Purposes 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 excessvie phlegm (mucus)

📄 Stop Use and Ask a Doctor If 53 words ▾

Stop use and consult 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 last 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 11 words ▾

Keep this and all drugs out of the reach of children.

📄 Other Information 23 words ▾

Other information 6 calories per drop May be useful for diabetics on the advise of a doctor Excessive consumption may cause laxative effect

📄 Questions or Comments 5 words ▾

Questions or comments call: 617-848-4560

📄 Package Label / Principal Display Panel 2 words ▾

Front Laqbel

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
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 Boston Nutraceutical Production SL. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Boston Nutraceutical Production SL 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.
← 72628-0102-01 · Boston 72628-0104-01 · Boston →
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.