Home › NDC Lookup › Ingredients › Brompheniramine Maleate,Dextromethorphan... › 82442-0536-08
📦image loading
(from DailyMed)

TARGET CHILDRENS DT AND NT COLD and COUGH Brompheniramine maleate,Dextromethorphan HBr,Phenylephrine HCl,Diphenhydramine HCl, Phenylephrine HCl Kit — NDC 82442-536-08 (Billing 82442-0536-08)

by TARGET CORPORATION · 1 KIT in 1 KIT * 118 mL in 1 BOTTLE, PLASTIC * 118 mL in 1 BOTTLE, PLASTIC

This is a package of TARGET CHILDRENS DT AND NT COLD and COUGH Brompheniramine maleate,Dextromethorphan HBr,Phenylephrine HCl,Diphenhydramine HCl, Phenylephrine HCl Kit from TARGET CORPORATION, marketed since Jun 2024 and currently FDA-listed. It is this product's only package size.

NDC 82442-0536-08
🏷️ FDA NDC (as labeled) 82442-536-08 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 82442-536-08 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
82442 labeler · 536 product · 08 package
Package marketed since
Jun 14, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8244253608 9
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 82442-536-08
Product NDC 82442-536
11-digit billing NDC 82442053608
RxCUI 1090463, 1236048, 1666116
Application # M012
SPL Set ID 05ac2a40-5eee-4013-b55b-6e370a28b21c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-06-14
Dosage form KIT
Quick answers
  • RxCUI (RxNorm): 1090463
Why two NDCs? The FDA registers this code as 82442-536-08 — 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 → 82442-0536-08. 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 Substituted alkylamines class.

Drug family (ATC) Substituted alkylamines
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

🧪 What is this product?

This is an over-the-counter kit product containing multiple active ingredients typically used to manage cold and cough symptoms. Brompheniramine maleate and diphenhydramine hydrochloride are antihistamines commonly used to reduce sneezing and runny nose. Dextromethorphan hydrobromide is a cough suppressant typically used to reduce coughing. Phenylephrine hydrochloride is a decongestant commonly used to help relieve nasal congestion. As an OTC monograph drug, this product is marketed under FDA's established rules for its category.

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
82442-0536-08 You're viewing this Main listing 1 KIT in 1 KIT * 118 mL in 1 BOTTLE, PLASTIC * 118 mL in 1 BOTTLE, PLASTIC 2024-06-14 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
TARGET CHILDRENS DT AND NT COLD and COUGHthis 82442-0536-08 TARGET 1 kit — — 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

🏛️
2024
On the market since
Jun 2024
📍
2026
Currently FDA-listed
2 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.

From the label’s inactive-ingredient sectionInactive ingredients for Day Time   anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose Inactive ingredients for Nighttime   anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

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

LabelerTARGET CORPORATION
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code82442
First marketedJun 2024
Product typeHuman Otc Drug
Portfolio409 products on file

More NDCs from TARGET CORPORATION labeler code 82442

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 📄 Ask a Doctor Before Use If 📄 Ask a Doctor or Pharmacist Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 59 words ▾

Uses Daytime temporarily relieves nasal congestion runny nose cough sneezing itching of the nose or throat itchy, watery eyes due to hay fever temporarily restores freer breathing through the nose. Nighttime temporarily relieves nasal congestion runny nose cough sneezing itching of the nose or throat itchy, watery eyes due to hay fever temporarily restores freer breathing through the nose.

⏱️ Dosage and Administration 119 words ▾

Directions Daytime do not take more than 6 doses in any 24-hour period measure only with dosing cup provided. Keep dosage cup with product mL= milliliter age dose Adults and children 12 years and over 20 mL every 4 hours children 6 to under 12 years 10 mL every 4 hours children under 6 years of age do not use Nighttime do not take more than 6 doses in any 24-hour period measure only with dosing cup provided. Keep dosage cup with product mL= milliliter age dose Adults and children 12 years and over 20 mL every 4 hours children 6 to under 12 years 10 mL every 4 hours children under 6 years of age do not use

⚠️ Warnings ~2 min read ▾

Warnings Do not use Daytime to sedate a child or to make a child sleepy if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your child's prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product. Nighttime only to sedate a child or to make a child sleepy if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug.

If you do not know if your child's prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product. With any other product containing diphenhydramine, even one used on skin Ask a doctor before use if you have DAYTIME heart disease high blood pressure diabetes thyroid disease trouble urinating due to an enlarged prostate gland glaucoma cough that occurs with too much phlegm (mucus) a breathing problem or chronic cough that lasts such as occurs with smoking, asthma, chronic bronchitis, or emphysema.

NIGHTTIME heart disease high blood pressure diabetes thyroid disease trouble urinating due to an enlarged prostate gland glaucoma cough that occurs with too much phlegm (mucus) a breathing problem or chronic cough that lasts such as occurs with smoking, asthma, chronic bronchitis, or emphysema. Ask a doctor or pharmacist before use if you are DAYTIME taking any other oral nasal decongestant or stimulant taking sedatives or tranquilizers NIGHTTIME taking any other oral nasal decongestant or stimulant taking sedatives or tranquilizers When using this product Daytime do not use more than directed. may cause marked drowsiness avoid alcohol, sedatives and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery excitability may occur, especially in children Nighttime do not use more than directed. may cause marked drowsiness avoid alcohol, sedatives and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery excitability may occur, especially in children Stop use and ask a doctor if DAYTIME nervousness, dizziness, or sleeplessness occur symptoms do not get better with 7 days or are accompanied with fever cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or headache.

These could be signs of a serious condition. NIGHTTIME nervousness, dizziness, or sleeplessness occur symptoms do not get better with 7 days or are accompanied with fever cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or headache. These could be signs of a serious condition.

Keep out of reach of children. Daytime In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222. Nighttime In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

📦 Storage and Handling 26 words ▾

Other information Daytime each 10 mL contains: sodium 6 mg store at room temperature. Nighttime each 10 mL contains: sodium 6 mg store at room temperature.

🧪 Active Ingredient 40 words ▾

Children’s Daytime Cold & Cough Active ingredients (in each 10 mL) Brompheniramine maleate, 2 mg Dextromethorphan HBr, 10 mg Phenylephrine HCl, 5 mg

Children’s Nighttime Cold & Congestion Active ingredients (in each 10 mL) Diphenhydramine HCL12.5 mg Phenylephrine HCL5 mg

🧪 Inactive Ingredients 57 words ▾

Inactive ingredients Inactive ingredients for Day Time anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose Inactive ingredients for Nighttime anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose

🎯 Purpose 23 words ▾

Purposes for Children’s Daytime Cold & Cough Antihistamine Cough suppressant Nasal decongestant

Purposes for Children’s Nighttime Cold & Congestion Antihistamine/Cough suppressant Nasal decongestant

📄 Ask a Doctor Before Use If 96 words ▾

Ask a doctor before use if you have DAYTIME heart disease high blood pressure diabetes thyroid disease trouble urinating due to an enlarged prostate gland glaucoma cough that occurs with too much phlegm (mucus) a breathing problem or chronic cough that lasts such as occurs with smoking, asthma, chronic bronchitis, or emphysema. NIGHTTIME heart disease high blood pressure diabetes thyroid disease trouble urinating due to an enlarged prostate gland glaucoma cough that occurs with too much phlegm (mucus) a breathing problem or chronic cough that lasts such as occurs with smoking, asthma, chronic bronchitis, or emphysema.

📄 Ask a Doctor or Pharmacist Before Use If 36 words ▾

Ask a doctor or pharmacist before use if you are DAYTIME taking any other oral nasal decongestant or stimulant taking sedatives or tranquilizers NIGHTTIME taking any other oral nasal decongestant or stimulant taking sedatives or tranquilizers

📄 When Using This Product 74 words ▾

When using this product Daytime do not use more than directed. may cause marked drowsiness avoid alcohol, sedatives and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery excitability may occur, especially in children Nighttime do not use more than directed. may cause marked drowsiness avoid alcohol, sedatives and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery excitability may occur, especially in children

📄 Stop Use and Ask a Doctor If 93 words ▾

Stop use and ask a doctor if DAYTIME nervousness, dizziness, or sleeplessness occur symptoms do not get better with 7 days or are accompanied with fever cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or headache. These could be signs of a serious condition. NIGHTTIME nervousness, dizziness, or sleeplessness occur symptoms do not get better with 7 days or are accompanied with fever cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or headache.

These could be signs of a serious condition.

🤰 If Pregnant or Breast-Feeding 10 words ▾

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

📄 Keep Out of Reach of Children 42 words ▾

Keep out of reach of children. Daytime In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222. Nighttime In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

📄 Questions or Comments 4 words ▾

Questions or comments? 1-866-467-2748

📄 Package Label / Principal Display Panel ~1 min read ▾

Principal Display Panel Compare to the active ingredients in Children's Dimetapp® Cold & Cough* Children's Daytime Cold & Cough Brompheniramine Maleate 2 mg (Antihistamine), Dextromethorphan HBr 10 mg (Cough Suppressant) Phenylephrine HCI 5 mg (Nasal Decongestant) Sneezing, stuffy or runny nose, cough, itchy or watery eyes No added alcohol Dosing Cup Included Ages 6+ Years Grape Flavor NATURALLY AND ARTIFICIALLY FLAVORED 4 FL OZ (118mL) Compare to the active ingredients in Children's Dimetapp® Nighttime Cold & Congestion** Children's Nighttime Cold & Congestion Diphenhydramine HCI 12.5 mg (Antihistamine / Cough Suppressant) Phenylephrine HCI 5 mg (Nasal Decongestant) Sneezing, stuffy or runny nose, cough, itchy or watery eyes No added alcohol Dosing Cup Included Ages 6+ Years Grape Flavor NATURALLY AND ARTIFICIALLY FLAVORED 4 FL OZ (118mL) 8 FL OZ (236 mL) TOTAL DO NOT TAKE BOTH PRODUCTS AT THE SAME TIME.

ALWAYS WAIT AT LEAST 4 HOURS BEFORE TAKING ANOTHER DOSE OF THE PRODUCT. TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND BOTTLE OR UNDER CAP IS BROKEN OR MISSING IMPORTANT: KEEP THIS CARTON FOR FUTURE REFERENCE FOR FULL LABELING *This product is not manufactured or distributed by Foundation Consumer Brands, LLC, the distributor of Children's Dimetapp® Cold & Congestion. Satisfaction guaranteed – Love it or your money back We welcome any questions you may have at Target.com/comments Or 1-800-910-6874.

Distributed by: Target Corporation Minneapolis, MN 55403 Made in the U.S.A. with domestic and imported ingredients TM & ©2024 Target Brands, Inc,

Product Label TARGET Children's Daytime & Nightime Cold & Cough Value pack

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

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 Brompheniramine maleate,Dextromethorphan HBr,Phenylephrine HCl,Diphenhydramine HCl, Phenylephrine HCl — the ingredient across all brands.

Top reported reactions

Hypersomnia1
Loss Of Consciousness1
Product Label Confusion1
Product Label Issue1
Product Packaging Confusion1
Somnolence1

Reporter sex

2 reports
Male · 50%
Female · 50%
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 2 0
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.

About this NDC listing & data coverage

Over-the-counter (OTC) product Kit / multi-component package

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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) ✓ 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 TARGET CORPORATION. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
TARGET CORPORATION 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.
← 82442-0532-78 · Target 82442-0546-71 · Target →
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.