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MGC Health Drops Sugar Free Lemon Mint MENTHOL 1.1 mg Lozenge, 25-count — NDC 83698-0132-25 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

MGC Health Drops Sugar Free Lemon Mint MENTHOL 1.1 mg Lozenge, 25-count — NDC 83698-132-25 (Billing 83698-0132-25)

by Xiamen Kang Zhongyuan Biotechnology Co., Ltd. · 25 LOZENGE in 1 BAG

This is a package of 25 lozenges of MGC Health Drops Sugar Free Lemon Mint MENTHOL 1.1 mg Lozenge from Xiamen Kang Zhongyuan Biotechnology Co., Ltd., marketed since Aug 2025 and currently FDA-listed. It is this product's only package size.

NDC 83698-0132-25
🏷️ FDA NDC (as labeled) 83698-132-25 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 83698-132-25 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
83698 labeler · 132 product · 25 package
Package marketed since
Aug 12, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8369813225 4
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) 83698-132-25
Product NDC 83698-132
11-digit billing NDC 83698013225
RxCUI 701201
UNII L7T10EIP3A
Application # M022
SPL Set ID b9227966-847c-40c3-87f2-8bea3954ec84
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-08-12
Route ORAL
Dosage form LOZENGE
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 701201
Why two NDCs? The FDA registers this code as 83698-132-25 — 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 → 83698-0132-25. 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
83698-0132-25 You're viewing this Main listing 25 LOZENGE in 1 BAG 2025-08-12 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
HyVee Throat Drops Lemon Mint 1.1 mg 42507-0907-25 HY-VEE, 25 lozenges — — FDA listed —
Lemon Mint Herb Throat Drops 1.1 mg 51316-0852-01 CVS 60 pastilles — — FDA listed —
Sugar Free Lemon Mint Herb Throat Drops 1.1 mg 54305-0102-19 Ricola 19 lozenges — — FDA listed —
Exchange Select Drops Sugar Free Lemon Mint 1.1 mg 55301-0586-25 Army 25 lozenges — — FDA listed —
Sugar Free Lemon Mint Herb Throat Drops 1.1 mg 63667-0956-19 Ricola 19 lozenges — — FDA listed —
Herbal Throat Drops Lemon Mint Herb 1.1 mg 76162-0060-01 Topco 45 pastilles — — FDA listed —
Herbal Throat Drops 1.1 mg 79481-0024-01 Meijer, 45 pastilles — — FDA listed —
Lemon Mint Drops 1.1 mg 82442-0202-01 Target 45 pastilles — — FDA listed —
MGC Health Drops Sugar Free Lemon Mint 1.1 mg 83173-0132-25 Medical 25 lozenges — — FDA listed —
MGC Health Drops Sugar Free Lemon Mint 1.1 mgthis 83698-0132-25 Xiamen 25 lozenges — — FDA listed —
Exchange Select Drops Sugar Free Lemon Mint 1.1 mg 83698-0586-25 Xiamen 25 lozenges — — FDA listed —
HyVee Throat Drops Lemon Mint 1.1 mg 83698-0907-25 Xiamen 25 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
Aug 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 yellow
ShapeOval
Size21 mm
ScoringNot scored
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.

🧪 Avoiding an ingredient? See Menthol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII PQ6CK8PD0R
    Ascorbic acid, also known as vitamin C, is a white crystalline powder. It serves as an antioxidant to prevent degradation of other ingredients and may also function as a preservative in the formulation.
  • UNII 01YAE03M7J
    Beta carotene is a naturally occurring orange pigment found in plants. In medicines, it serves as a colorant to make tablets or capsules appear orange or yellow.
  • 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 K08036XEJV
    Horehound is a plant extract used as a flavoring agent in medicines. It adds a distinctive bitter or minty taste to help mask unpleasant flavors in syrups and lozenges.
  • UNII X7HKN4FOJI
    A plant extract from hyssop flowers, traditionally used in herbal preparations. It may function as a flavoring agent, fragrance, or botanical extract to add therapeutic or sensory qualities to the medicine.
  • 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 MJ76269K9S
    Lemon balm oil is a natural essential oil extracted from the lemon balm plant. In medicines, it typically serves as a flavoring agent and fragrance to improve taste and aroma.
  • UNII 817L1N4CKP
    Malic acid is a naturally occurring organic acid found in fruits. It works as a buffer and flavor agent to maintain the medicine's pH balance and add tartness to the product.
  • 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 17H39B00T5
    A plant extract from common mallow leaves used as a natural flavoring agent and skin-conditioning ingredient in some formulations. It may help provide mild taste or texture qualities to the medicine.
  • UNII 5QUO05548Z
    Palm oil is a natural plant-based fat extracted from palm fruit. It's used as a lubricant, binder, or coating agent to help the medicine hold together, flow smoothly during manufacturing, and sometimes improve how the body absorbs the active ingredient.
  • UNII V95R5KMY2B
    Peppermint is a flavoring agent derived from the peppermint plant. It's added to medicines to improve taste and mask bitter or unpleasant flavors, making them easier to take.
  • UNII 065C5D077J
    Sage is a natural plant extract used in medicines as a flavoring agent and preservative. It may help mask bitter tastes and extend shelf life in certain formulations.
  • UNII 07V4DX094T
    Sambucus nigra flower is an extract from the black elderflower plant. It may be added to medicines as a flavoring or coloring agent, or to provide traditional herbal characteristics to the formulation.
  • 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 CW657OBU4N
    A plant extract from thyme used as a flavoring agent and preservative in medicines. It adds taste and aroma while helping protect the product from spoilage.
  • UNII CFN6G1F6YK
    A plant extract from small-leaved linden flowers, used as a flavoring agent and natural coloring ingredient to improve taste and appearance in medicines.
  • UNII KXK6I80R8W
    Wild thyme is a plant extract used in medicines as a flavoring and aromatic agent. It may also provide mild antimicrobial or soothing properties to the formulation.

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

The official label also statesascorbic acid (vitamin C), citric acid, flavors, Herbal extract blend (elderflower extract, horehound extract, hyssop extract, lemon balm extract, linden flower extract, malva sylvestris (mallow) leaf extract, peppermint extract, sage extract, thyme extract, wild thyme extract), isomalt, malic acid, maltitol, natural color (beta-carotene), palm oil, soy lecithin, sucralose.

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

LabelerXiamen Kang Zhongyuan Biotechnology Co., Ltd.
FDA applicationM022 (OTC MONOGRAPH DRUG)
Labeler code83698
First marketedAug 2025
Product typeHuman Otc Drug
Portfolio68 products on file

More NDCs from Xiamen Kang Zhongyuan Biotechnology Co., Ltd. labeler code 83698

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 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 15 words ▾

Uses for the temporary relief of occasional minor irritation, pain, sore mouth, and sore throat

⏱️ Dosage and Administration 48 words ▾

Directions Adults and children 2 years of age and older: Dissolve 2 drops (1 at a time) slowly in the mouth. May be repeated every 2 hours as needed or as directed by a dentist or doctor. Children under 2 years of age: Consult a dentist or doctor.

⚠️ Warnings 31 words ▾

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, 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 8 words ▾

Active Ingredient (in each drop) Menthol, 1.1 mg

🧪 Inactive Ingredients 50 words ▾

Inactive Ingredients ascorbic acid (vitamin C), citric acid, flavors, Herbal extract blend (elderflower extract, horehound extract, hyssop extract, lemon balm extract, linden flower extract, malva sylvestris (mallow) leaf extract, peppermint extract, sage extract, thyme extract, wild thyme extract), isomalt, malic acid, maltitol, natural color (beta-carotene), palm oil, soy lecithin, sucralose.

🎯 Purpose 5 words ▾

Drug Facts Purpose Oral anesthetic

📄 When Using This Product 9 words ▾

When using this product do not exceed recommended dosage

📄 Keep Out of Reach of Children 11 words ▾

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

📄 Questions or Comments 22 words ▾

Questions or comments? Call +1-866-306-9136 You may also report concerns to this phone number Monday-Friday, 9 AM - 5 PM EASTERN TIME

📄 Package Label / Principal Display Panel 2 words ▾

image description

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 Xiamen Kang Zhongyuan Biotechnology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. 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.
← 83698-0131-30 · Xiamen 83698-0134-96 · Xiamen →
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.