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Meclizine HCL 25 mg 25 mg Tablet, 1,000-count — NDC 69618-028-10 (Billing 69618-0028-10)

by Reliable 1 Laboratories LLC · 1000 TABLET in 1 BOTTLE, PLASTIC

This is a package of 1,000 tablets of Meclizine HCL 25 mg 25 mg Tablet from Reliable 1 Laboratories LLC, marketed since Nov 2015 and currently FDA-listed.

NDC 69618-0028-10
🏷️ FDA NDC (as labeled) 69618-028-10 billing pads the product segment with a zero
This package
Contains1,000-count Pack sizes2 compare ↓
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 →

NDC database record

One package, one record: these facts belong to NDC 69618-028-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69618 labeler · 028 product · 10 package
Package marketed since
Nov 1, 2015
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Billing quantity
1,000 EA per package
Barcode (UPC)
0369618028104
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69618-028-10
Product NDC 69618-028
11-digit billing NDC 69618002810
NCPDP billing unit EA — each (per item)
RxCUI 995632
UNII HDP7W44CIO
UPC 0369618028104
Application # M009
SPL Set ID 32bdd802-16b0-184d-e054-00144ff88e88
Established class (EPC) Antiemetic
Physiologic effect Emesis Suppression
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-11-01
Route ORAL
Dosage form TABLET
Substance MECLIZINE HYDROCHLORIDE

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 50200050000510
GPI class Meclizine HCl
GCN Seq No 004736
GCN 18312
HICL code 001975
Ingredient (HICL) Meclizine Hcl
HIC1 code H
Therapeutic class — broad (HIC1) Nervous System (Except Autonomic)
HIC2 code H6
Therapeutic class — intermediate (HIC2) Drugs Acting Principally On The Midbrain
HIC3 code H6J
Therapeutic class — specific (HIC3) Antiemetic/Antivertigo Agents
AHFS code 04:04.16.00
AHFS class Piperazine Derivatives
FDB label name MECLIZINE 25 MG TABLET CHEW
FDB brand name Meclizine Hcl
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 004736
  • GCN: 18312
  • GPI-14 (Medi-Span): 50200050000510
  • HICL (First Databank): 001975
  • AHFS class code: 04:04.16.00
  • RxCUI (RxNorm): 995632
Why two NDCs? The FDA registers this code as 69618-028-10 — 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 → 69618-0028-10. 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.

RxNorm drug class

This medicine belongs to the Antiemetic class.

Pharmacologic class Antiemetic
Drug family (ATC) Piperazine derivatives
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

Label name MECLIZINE 25 MG TABLET CHEW Ingredient Meclizine Hcl
📗 Our plain-language guide HelloPharmacist
  • Meclizine is mainly used to prevent and treat the nausea, vomiting, and dizziness that comes with motion sickness — whether you're on a boat, in a car, or on a plane. It's also use...
  • For the best chance of preventing motion sickness, take meclizine about one hour before you start traveling. After that first dose, you can take it once every 24 hours as needed fo...
  • Yes, drowsiness is the most common side effect — it's actually worth planning around. Avoid driving or operating heavy machinery until you know how it affects you. And definitely s...
  • This one requires a conversation with your doctor. Human studies haven't clearly linked meclizine to birth defects, but animal studies did show fetal harm at doses similar to what...
📖 Read our full Meclizine guide →
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: 100 tablets
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
69618-0028-01 69618-028-01 Main listing 100 TABLET in 1 BOTTLE, PLASTIC 2015-11-01 — Active
69618-0028-10 You're viewing this 1000 TABLET in 1 BOTTLE, PLASTIC 2015-11-01 — Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 1,000-count package — 1000 tablet in 1 bottle, plastic.
How does this package differ from NDC 69618-0028-01?
Both are Meclizine HCL 25 mg 25 mg Tablet — the drug itself is identical. This page's package is the 1,000-count one, while NDC 69618-0028-01 is the 100 tablets package.
What NDC number is used to bill for this package of Meclizine HCL 25 mg 25 mg Tablet?
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
Meclizine Hydrochloride 25 mg 00536-1299-01 Rugby 100 tablets $0.033 — Availability likely —
Meclizine HCl 25 mg 16571-0824-01 Rising 100 tablets $0.033 — Availability likely —
Motion Sickness Relief 25 mg 46122-0774-51 Amerisource 8 tablets $0.033 — Availability likely —
Motion-Time Chewable 25 mg/251 49483-0333-01 Time-Cap 100 tablets $0.033 — Availability likely —
Meclizine HCl 25 mg 68001-0529-00 BluePoint 100 tablets $0.033 — Availability likely —
Motion Sickness 25 mg 70677-1290-01 Strategic 100 tablets $0.033 — Availability likely —
Travel ease 25 mg 83324-0027-16 Chain 8 tablets $0.033 — Availability likely —
Motion Sickness 25 mg 70677-1088-01 Strategic 8 tablets $0.128 — Availability likely —
Motion Sickness Relief 25 mg 46122-0535-51 Amerisource 8 tablets $0.128 — Availability likely —
Motion Sickness Relief 25 mg 70000-0097-01 Cardinal 32 tablets $0.128 — Availability likely —
Motion Sickness Relief 25 mg 00363-4040-21 Walgreen 8 tablets — — FDA listed —
Meclizine Hydrochloride 25 mg 00363-5172-07 Walgreen 12 tablets — — FDA listed —
Motion Sickness Relief 25 mg 11822-4040-01 Rite 8 tablets — — FDA listed —
Meclizine 25 mg 16103-0387-08 Pharbest 100 tablets — — FDA listed —
Meclizine Hydrochloride 25 mg 16571-0663-01 Rising 100 tablets — — FDA listed —
Meclizine HCL 25 mg 17714-0115-01 Advance 100 tablets — — FDA listed —
Meclizine 25 mg 37835-0202-01 Bi-Mart 100 tablets — — FDA listed —
Meclizine 25 mg 43063-0804-01 PD-Rx 100 tablets — — FDA listed —
Meclizine Hydrochloride 25 mg 50090-5496-00 A-S 30 tablets — — FDA listed —
Meclizine Hydrochloride 25 mg 50090-5952-00 A-S 30 tablets — — FDA listed —
Motion Sickness Relief 25 mg 51013-0322-54 PuraCap 2 tablets — — FDA listed —
Motion Sickness Relief 25 mg 51316-0404-21 CVS 8 tablets — — FDA listed —
Motion Sickness 25 mg 51316-0441-21 CVS 8 tablets — — FDA listed —
Meclizine HCL 25 mg 54738-0025-01 Richmond 100 tablets — — FDA listed —
Dramamine 25 mg 63029-0906-12 Medtech 12 tablets — — FDA listed —
Dramamine 25 mg 63029-0913-12 Medtech 12 tablets — — FDA listed —
Dramamine 25 mg 63029-0914-12 Medtech 12 tablets — — FDA listed —
Bonine 25 mg 65197-0275-02 WellSpring 2 tablets — — FDA listed —
Bonine 25 mg 65197-0296-08 WellSpring 8 tablets — — FDA listed —
Bonine 25 mg 65197-0297-08 WellSpring 8 tablets — — FDA listed —
Meclizine Hydrochloride 25 mg 68071-2574-02 NuCare 20 tablets — — FDA listed —
Meclizine HCL 25 mg 68788-7982-01 Preferred 10 tablets — — FDA listed —
Meclizine HCl 25 mg 68788-8529-01 Preferred 10 tablets — — FDA listed —
Meclizine HCL 25 mgthis 69618-0028-10 Reliable 1000 tablets — — FDA listed —
Motion Sickness Relief 25 mg 69842-0395-54 CVS 2 tablets — — FDA listed —
Meclizine HCL 25 mg 71205-0606-30 Proficient 30 tablets — — FDA listed —
Meclizine 25 mg 71335-1215-00 Bryant 120 tablets — — FDA listed —
Meclizine HCL 25 mg 71335-1607-00 Bryant 120 tablets — — FDA listed —
Meclizine Hydrochloride 25 mg 71335-2177-00 Bryant 120 tablets — — FDA listed —
Meclizine HCl 25 mg 71335-9751-00 Bryant 120 tablets — — FDA listed —
Meclizine HCL 25 mg 71610-0528-30 Aphena 30 tablets — — FDA listed —
Meclizine Hydrochloride 25 mg 71610-0836-30 Aphena 30 tablets — — FDA listed —
Meclizine Hydrochloride 25 mg 72789-0250-12 PD-Rx 12 tablets — — FDA listed —
Meclizine 25 mg 80513-0421-02 Advanced 200 tablets — — FDA listed —
Travel-Ease 25 mg 57896-0378-01 Geri-Care 100 tablets — — FDA listed —
Motion Sickness Relief 25 mg 55910-0943-19 DOLGENCORP, 8 tablets — — FDA listed —
Nausea Relief 25 mg 79903-0177-10 WALMART 10 tablets — — FDA listed —
Motion Sickness Relief 25 mg 83059-0007-01 Shield 15 tablets — — FDA listed —
Motion Sickness Relief 25 mg 55319-0903-19 Family 8 tablets — — FDA listed —
Motion Sickness Relief 25 mg 00363-4030-21 Walgreen 16 tablets — — FDA listed —
Motion Sickness Relief 25 mg 30142-0943-19 Kroger 8 tablets — — FDA listed —
Less Drowsy Motion Sickness Relief 25 mg 49035-0403-19 Wal-Mart 8 tablets — — FDA listed —
Motion Sickness 25 mg 55301-0403-21 ARMY 16 tablets — — FDA listed —
Less Drowsy Formula Motion Sickness Relief 25 mg 57243-0403-02 Salado 12 tablets — — FDA listed —
Motion Sickness Relief Less Drowsy 25 mg 21130-0778-02 Better 12 tablets — — FDA listed —
Motion Sickness Relief 25 mg 41250-0930-19 Meijer 8 tablets — — FDA listed —
Medique Medi-Meclizine 25 mg 47682-0481-15 Unifirst 1000 tablets — — FDA listed —
Motion Sickness Relief 25 mg 36800-0943-19 Topco 8 tablets — — FDA listed —
Motion Sickness Relief 25 mg 41163-0304-02 United 12 tablets — — FDA listed —
Medique Medi-Meclizine 25 mg 85766-0175-00 Sportpharm 1000 tablets — — FDA listed —
Motion Sickness Relief 25 mg 50844-0403-19 L.N.K. 8 tablets — — FDA listed —
PhysiciansCare Motion Sickness 25 mg 00924-1008-00 Acme 2 tablets — — FDA listed —
Less Drowsy Motion Sickness Relief 25 mg 11822-0775-09 Rite 8 tablets — — FDA listed —
Pepto Nausea Motion Sickness 25 mg 84126-0340-01 THE 10 tablets — — FDA listed —
Motion Sickness 25 mg 37808-0903-12 H 100 tablets — — FDA listed —
Pepto Motion Sickness 25 mg 84126-0380-01 THE 10 tablets — — 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

🏛️
2015
On the market since
Nov 2015
📍
2026
Currently FDA-listed
11 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.

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.

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

LabelerReliable 1 Laboratories LLC
FDA applicationM009 (OTC MONOGRAPH DRUG)
Labeler code69618
First marketedNov 2015
Product typeHuman Otc Drug
Portfolio26 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 18 words ▾

Uses prevents and treats nausea, vomiting or dizziness due to motion sickness for others uses, consult your doctor

⏱️ Dosage and Administration 35 words ▾

Directions take dose one hour before travel starts tablets can be chewed or swallowed whole with water adults & children 12 years and over: 1-2 tablets once daily children unser 12 years: ask a doctor

⚠️ Warnings 100 words ▾

Warnings Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers When using this prodcut you may get drowsy avoid alcoholic drinks alcohol, sedatives and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.

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

🧪 Active Ingredient 9 words ▾

Active ingredient (in each tablet) Meclizine HCL 25 mg

🧪 Inactive Ingredients 19 words ▾

Inactive ingredients aspartame, compressible sugar, croscarmellose sodium, dextrose, FD&C red # 40 (Al-lake), magnesium stearate, microcrystalline cellulose, raspberry flavor

🎯 Purpose 2 words ▾

Purpose Antiemetic

📄 Ask a Doctor Before Use If 26 words ▾

Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland

📄 Ask a Doctor or Pharmacist Before Use If 14 words ▾

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

📄 When Using This Product 28 words ▾

When using this product you may get drowsy avoid alcoholic drinks alcohol, sedatives and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery

🤰 If Pregnant or Breast-Feeding 10 words ▾

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

📄 Keep Out of Reach of Children 21 words ▾

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 14 words ▾

Questions or comments? call 516-341-0666, 8:30 am - 4:30 pm ET, Monday - Friday

📄 Package Label / Principal Display Panel 26 words ▾

NDC 69618-028-10 Meclizine HCL 25 mg ANTIEMETIC 1000 TABLETS THIS PACKAGE FOR HOUSEHOLD WITHOUT YOUNG CHILDREN *Compare to Active Ingredient in BONINE® MECLIZINE HCL 25 MG

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

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Meclizine HCl (matched by generic name) — the program that covers self-administered drugs. 8 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Meclizine HCl. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$6.73M
Claims incl. refills
748.9K
Beneficiaries
532.6K
Spend / beneficiary
$12.64
Spend / claim
$8.99
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

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 — 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.
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 Reliable 1 Laboratories LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 100 tablets (69618-0028-01). 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?
Reliable 1 Laboratories LLC 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.