Allergy Chlorpheniramine Maleate 4 mg Tablet, 100-count
by Bi-Mart · 100 TABLET in 1 BOTTLE (37835-633-01)
NDC 37835-0633-01
🏷️ FDA NDC (as labeled)
37835-633-01
billing pads the product segment with a zero
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 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)
37835-633-01
Product NDC
37835-633
11-digit billing NDC
37835063301
RxCUI
1363309
UNII
V1Q0O9OJ9Z
UPC
0071357002047
Application #
M012
SPL Set ID
922ec870-79d5-46be-80d8-20fb0ecd823b
Established class (EPC)
Histamine-1 Receptor Antagonist
Mechanism of action
Histamine H1 Receptor Antagonists
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-02-01
Route
ORAL
Dosage form
TABLET
Substance
CHLORPHENIRAMINE MALEATE
Why two NDCs?
The FDA registers this code as 37835-633-01 — 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 → 37835-0633-01. 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.
🏷️ RxNorm drug class
This medicine belongs to the Histamine-1 Receptor Antagonist class.
Pharmacologic class
Histamine-1 Receptor Antagonist
Drug family (ATC)
Substituted alkylamines
How it works
Histamine H1 Receptor Antagonists
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.
🏭 Manufacturer & labeler
LabelerBi-Mart
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code37835
First marketedFeb 2026
Product typeHuman Otc Drug
Portfolio58 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 it is MedlinePlus · NLM
Chlorpheniramine is used to treat allergy symptoms: sneezing runny nose itchy nose or throat red, itchy, watery eyes Chlorpheniramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
Read the full MedlinePlus article ↗📗 Our plain-language guide HelloPharmacist
- It's an antihistamine used to temporarily relieve classic hay fever and allergy symptoms — things like a runny nose, sneezing, itchy or watery eyes, and an itchy throat. It works o...
- What is chlorpheniramine actually used for?
- Yes — drowsiness is one of the most common effects of chlorpheniramine, and it can be significant. Don't plan on driving or operating heavy machinery until you know how your body r...
- It's best to skip the alcohol while you're taking chlorpheniramine. Alcohol makes the drowsiness much stronger, which can be unsafe — especially if you need to drive or stay alert....
Patient education
Supplement & herbal interactions
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 Chlorpheniramine Maleate?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
yellow
ShapeRound
ImprintPH012
Size8 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 L11K75P92J
A mineral salt made from calcium and phosphate. It acts as a filler and binder in tablets to add bulk and help hold the medicine together in solid form.
-
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 CQ3XH3DET6
D&C Yellow No. 10 Aluminum Lake is a yellow colorant made by combining a dye with aluminum salts. It's used in medicines to add color for product identification and visual appeal.
-
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 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.
7 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statescorn starch, croscarmellose sodium, D&C yellow # 10 aluminum lake, dicalcium phosphate, magnesium stearate, microcrystalline cellulose, silicon 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 |
|---|---|---|---|---|---|---|
| Allergy Relief 4 Hour 4 mg 70000-0160-01 | Cardinal | 24 tablets | $0.018 | — | Discontinued | — |
| Allergy 4 mg 00904-0012-24 | Major | 24 tablets | $0.018 | — | Availability likely | — |
| Allergy Relief 4 mg 46122-0618-62 | Amerisource | 24 tablets | $0.018 | — | Availability likely | — |
| Allergy Relief 4 mg 70677-1016-01 | Strategic | 100 tablets | $0.018 | — | Availability likely | — |
| Allergy Relief 4 mg 83324-0068-24 | Chain | 24 tablets | $0.018 | — | Availability likely | — |
| Aller-chlor 4 mg 00536-1006-01 | Rugby | 100 tablets | $0.018 | — | Availability likely | — |
| Allergy Relief 4 mg 00363-1941-15 | Walgreen | 50 tablets | — | — | FDA listed | — |
| allergy relief 4 mg 11822-0662-01 | Rite | 100 tablets | — | — | FDA listed | — |
| Anti Allergy 4 mg 17714-0016-01 | Advance | 100 tablets | — | — | FDA listed | — |
| Allergy Relief 4 mg 36800-0694-08 | Topco | 24 tablets | — | — | FDA listed | — |
| Allergy 4 mgthis 37835-0633-01 | Bi-Mart | 100 tablets | — | — | FDA listed | — |
| Allergy 4 mg 41163-0194-08 | United | 24 tablets | — | — | FDA listed | — |
| Medique Chlorphen 4 mg 47682-0169-46 | Unifirst | 1 tablet | — | — | FDA listed | — |
| Allergy Time 4 mg 49483-0242-00 | Time | 100000 tablets | — | — | FDA listed | — |
| Allergy 4 mg 50090-0049-00 | A-S | 100 tablets | — | — | FDA listed | — |
| Allergy Relief 4 mg 50804-0277-93 | Good | 24 tablets | — | — | FDA listed | — |
| Sprinsol 4 mg 51467-0101-01 | FORTUNE | 24 tablets | — | — | FDA listed | — |
| Chlorpheniramine maleate 4mg 4 mg 53185-0277-24 | Athlete's | 24 tablets | — | — | FDA listed | — |
| Anti Allergy 4 mg 54738-0103-01 | Richmond | 100 tablets | — | — | FDA listed | — |
| Chlorpheniramine Maleate 4 mg 55289-0560-01 | PD-Rx | 100 tablets | — | — | FDA listed | — |
| Allergy Relief 4 Hour 4 mg 57896-0974-01 | Geri-Care | 100 tablets | — | — | FDA listed | — |
| Allergy Relief 4 mg 63868-0333-24 | CHAIN | 24 tablets | — | — | FDA listed | — |
| Allergy Relief 4 Hour 4 mg 67091-0203-24 | WinCo | 24 tablets | — | — | FDA listed | — |
| Allergy Relief 4 mg 68016-0683-81 | Chain | 100 tablets | — | — | FDA listed | — |
| Allergy 4 mg 68998-0277-93 | Marc | 24 tablets | — | — | FDA listed | — |
| Allergy 4 mg 69168-0277-93 | Allegiant | 24 tablets | — | — | FDA listed | — |
| Allergy Relief 4 mg 69842-0194-12 | CVS | 100 tablets | — | — | FDA listed | — |
| Chlorpheniramine Maleate 4 mg 71335-0963-01 | Bryant | 30 tablets | — | — | FDA listed | — |
| Allergy 4 mg 71335-2056-01 | Bryant | 30 tablets | — | — | FDA listed | — |
| Allergy Relief 4 mg 71335-2812-01 | Bryant | 100 tablets | — | — | FDA listed | — |
| Allergy Relief 4 Hour 4 mg 71335-3093-01 | Bryant | 30 tablets | — | — | FDA listed | — |
| Pharbechlor 4 mg 73057-0346-11 | Ulai | 1000 tablets | — | — | FDA listed | — |
| Allergy Relief 4 mg 79903-0074-12 | WALMART | 100 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
Feb 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 allergy (this brand).
Top reported reactions
Reporter sex
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 |
|---|---|---|---|
| 37835-0633-01 You're viewing this | 100 TABLET in 1 BOTTLE (37835-633-01) | 2026-02-01 | 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 37835-633-01, 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: 37835-0633-01, written without dashes as 37835063301. 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 37835-0633-01, the first segment (37835) is the labeler code FDA assigned to Bi-Mart; the middle segment (0633) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Bi-Mart. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Bi-Mart 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.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses temporarily relieves the following symptoms due to hay fever and other upper respiratory allergies: sneezing itchy, watery eyes runny nose itching of the nose and throat
⏱️ Dosage and Administration ▾
Directions adults and children 12 years of age and over 1 tablet every 4 to 6 hours, not to exceed 6 tablets in 24 hours. children 6 to under 12 years of age 1/2 tablet (break tablet in half) every 4 to 6 hours, not to exceed 3 whole tablets in 24 hours. children under 6 years of age ask a doctor
⚠️ Warnings ▾
Warnings Do not use to make a child sleepy.
📦 Storage and Handling ▾
Other information store at 15 o -25 o C (59 o -77 o F) protect from moisture
🧪 Active Ingredient ▾
Active ingredient (in each tablet) Chlorpheniramine maleate 4 mg
🧪 Inactive Ingredients ▾
Inactive ingredients corn starch, croscarmellose sodium, D&C yellow # 10 aluminum lake, dicalcium phosphate, magnesium stearate, microcrystalline cellulose, silicon dioxide.
🎯 Purpose ▾
Purpose Antihistamine
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.