Menstrual Complete Acetaminophen, Caffeine, Pyrilamine Maleate 500 mg; 60 mg; 15 mg Tablet, 40-count
by Kroger · 1 BOTTLE in 1 CARTON (41226-348-44) / 40 TABLET in 1 BOTTLE
NDC 41226-0348-44
🏷️ FDA NDC (as labeled)
41226-348-44
billing pads the product segment with a zero
OTC
On market
Non-controlled
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
41226-348-44
Product NDC
41226-348
11-digit billing NDC
41226034844
Application #
M013
SPL Set ID
514a9340-b88c-2167-e063-6294a90a4165
Established class (EPC)
Central Nervous System Stimulant; Methylxanthine
Physiologic effect
Central Nervous System Stimulation
Chemical class
Xanthines
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-09-15
Route
ORAL
Dosage form
TABLET
Substance
ACETAMINOPHEN; CAFFEINE; PYRILAMINE MALEATE
Why two NDCs?
The FDA registers this code as 41226-348-44 — 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 → 41226-0348-44. 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.
🏭 Manufacturer & labeler
LabelerKroger
FDA applicationM013 (OTC MONOGRAPH DRUG)
Labeler code41226
First marketedSep 2026
Product typeHuman Otc Drug
Portfolio36 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.
🩺 Clinical
🧪 What is this product?
Menstrual Complete is an over-the-counter tablet taken by mouth that combines three active ingredients commonly used together during menstrual discomfort. Acetaminophen functions as a pain reliever and fever reducer. Caffeine is typically added to enhance pain relief and help counteract fatigue. Pyrilamine maleate is an antihistamine commonly included in menstrual products to help reduce bloating and other associated symptoms.
Patient education
Supplement & herbal interactions
7
Nutrient depletion considerations
Acetaminophen, Caffeine, Pyrilamine may be associated with lower levels of 7 nutrients — worth a chat with your pharmacist, not a cause for alarm.
POTASSIUM
Major Depletion
VITAMIN C
Insignificant Depletion
MAGNESIUM
Moderate Depletion
THIAMINE
Moderate Depletion
FOLIC ACID
Insufficient Evidence
+2 more
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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.
💬 Questions about Acetaminophen, Caffeine, Pyrilamine Maleate?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
white
ShapeCapsule
ImprintTCL347
Size18 mm
ScoringNot scored
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 M28OL1HH48
Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
-
UNII 2S7830E561
Crospovidone is a synthetic polymer derived from povidone. It acts as a disintegrant, helping the tablet or capsule break apart quickly in the stomach so the active ingredient can be absorbed.
-
UNII 3NXW29V3WO
Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
-
UNII 70097M6I30
Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
-
UNII OP1R32D61U
Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
-
UNII T5L8T28FGP
Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
-
UNII FZ989GH94E
Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
-
UNII ETJ7Z6XBU4
Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
-
UNII O8232NY3SJ
A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
-
UNII 4ELV7Z65AP
Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
-
UNII 15FIX9V2JP
Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
11 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesInactive ingredients colloidal silicon dioxide, croscarmellose sodium, crospovidone, hypromellose, magnesium stearate, microcrystalline cellulose, mineral oil, povidone, pregelatinized starch, stearic acid, titanium dioxide
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.
💲 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.
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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Midol Complete 500 mg/1; 60 mg/1; 15 mg 50269-0007-06 | JC | 12 tablets | — | — | FDA listed | — |
| Midol Complete 500 mg/1; 60 mg/1; 15 mg 50269-0009-06 | JC | 24 tablets | — | — | FDA listed | — |
| FLO PMS Complete 500 mg/1; 60 mg/1; 15 mg 83049-0489-08 | O | 24 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 79903-0266-40 | WALMART | 40 tablets | — | — | FDA listed | — |
| Syncol Max 500 mg/1; 60 mg/1; 15 mg 83393-0390-02 | Laboratorios | 12 tablets | — | — | FDA listed | — |
| Multi-Symptom Menstrual Relief 500 mg/1; 60 mg/1; 15 mg 11673-0363-64 | TARGET | 40 tablets | — | — | FDA listed | — |
| Menstrual Complete Maximum Strength 500 mg/1; 60 mg/1; 15 mg 63868-0032-24 | CHAIN | 24 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 79481-0390-01 | Meijer | 40 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 83324-0017-24 | Chain | 24 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 11822-3900-01 | Rite | 40 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 36800-0391-08 | Topco | 24 tablets | — | — | FDA listed | — |
| Menstrual Relief 500 mg/1; 60 mg/1; 15 mg 59779-0930-08 | CVS | 8 tablets | — | — | FDA listed | — |
| Menstrual Relief 500 mg/1; 60 mg/1; 15 mg 41163-0391-10 | United | 40 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 53943-0390-10 | Discount | 40 tablets | — | — | FDA listed | — |
| Menstrual Complete Pain Relief 500 mg/1; 60 mg/1; 15 mg 00363-9390-10 | Walgreen | 40 tablets | — | — | FDA listed | — |
| Menstrual Relief 500 mg/1; 60 mg/1; 15 mg 21130-0930-10 | Better | 40 tablets | — | — | FDA listed | — |
| Menstrual Relief 500 mg/1; 60 mg/1; 15 mg 50804-0990-08 | Geiss, | 24 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 50844-0399-08 | L.N.K. | 24 tablets | — | — | FDA listed | — |
| Menstrual Pain Relief 500 mg/1; 60 mg/1; 15 mg 00363-3900-10 | Walgreen | 40 tablets | — | — | Discontinued | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 37808-0389-10 | H | 40 tablets | — | — | FDA listed | — |
| Menstrual Relief 500 mg/1; 60 mg/1; 15 mg 51316-0390-10 | CVS | 40 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 30142-0390-10 | Kroger | 40 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 67091-0334-40 | WinCo | 40 tablets | — | — | FDA listed | — |
| Buscapina 500 mg/1; 60 mg/1; 15 mg 69729-0131-72 | OPMX | 2 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 55319-0301-21 | Family | 8 tablets | — | — | FDA listed | — |
| Dolex Fem 500 mg/1; 60 mg/1; 15 mg 55758-0326-25 | Pharmadel | 24 tablets | — | — | FDA listed | — |
| Menstrual Relief 500 mg/1; 60 mg/1; 15 mg 00363-3909-21 | Walgreen | 8 tablets | — | — | FDA listed | — |
| Buscapina 500 mg/1; 60 mg/1; 15 mg 69729-0130-24 | OPMX | 24 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mg 70692-0131-24 | Strive | 24 tablets | — | — | FDA listed | — |
| Menstrual Complete 500 mg/1; 60 mg/1; 15 mgthis 41226-0348-44 | Kroger | 40 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
🏛️
2026
On the market since
Sep 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.
🔬 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 Menstrual Complete (this brand).
Top reported reactions
Reporter sex
Female · 100%
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 41226-0348-44 You're viewing this | 1 BOTTLE in 1 CARTON (41226-348-44) / 40 TABLET in 1 BOTTLE | 2026-09-15 | Active |
🧭 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 FDA registers it as 41226-348-44, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 41226-0348-44, written without dashes as 41226034844. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 41226-0348-44, the first segment (41226) is the labeler code FDA assigned to Kroger; the middle segment (0348) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (44) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Kroger. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Kroger 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.
📄 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.
📄 FDA label ▾
No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.
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 ↗
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.