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Walgreens DAY and NIGHT PACK Dextromethorphan HBr, Guaifenesin, Chlorpheniramine maleate Kit — NDC 00363-7570-08 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Walgreens DAY and NIGHT PACK Dextromethorphan HBr, Guaifenesin, Chlorpheniramine maleate Kit — NDC 0363-7570-08 (Billing 00363-7570-08)

by WALGREEN CO · 1 KIT in 1 KIT * 118 mL in 1 BOTTLE * 118 mL in 1 BOTTLE

This is a package of Walgreens DAY and NIGHT PACK Dextromethorphan HBr, Guaifenesin, Chlorpheniramine maleate Kit from WALGREEN CO, marketed since Apr 2020 and currently FDA-listed. It is this product's only package size.

NDC 00363-7570-08
🏷️ FDA NDC (as labeled) 0363-7570-08 billing pads the labeler 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 0363-7570-08 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
0363 labeler · 7570 product · 08 package
Package marketed since
Apr 13, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0311917177007
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0363-7570-08
Product NDC 0363-7570
11-digit billing NDC 00363757008
RxCUI 1111440, 1790650, 2362250
UPC 0311917177007
Application # M012
SPL Set ID cb87e57b-ff06-4973-9751-137c7021e272
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-04-13
Dosage form KIT
Quick answers
  • RxCUI (RxNorm): 1111440
Why two NDCs? The FDA registers this code as 0363-7570-08 — a 4-4-2 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 labeler segment → 00363-7570-08. 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 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.

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 helps loosen mucus and makes coughs more productive. It also temporarily eases cough from minor throat and bronchial irritation, like with a cold or inhaled irritants.
  • Swallow them whole with a full glass of water. Don’t crush, chew or break them. You can take them with or without food, about every 12 hours as your label directs.
  • How do I take the extended-release tablets?
  • The extended-release tablets are not for children under 12. Some liquid products are made for children, so check that product’s label and ask me if you’re unsure.
📖 Read our full Dextromethorphan / Guaifenesin 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
00363-7570-08 You're viewing this Main listing 1 KIT in 1 KIT * 118 mL in 1 BOTTLE * 118 mL in 1 BOTTLE 2020-04-13 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Kids Daytime Cough and Nighttime Cough combo pack 69676-0110-09 Genexa 2 bottles — — FDA listed —
Walgreens DAY and NIGHT PACKthis 00363-7570-08 WALGREEN 1 kit — — FDA listed —
Daytime and Nighttime Cough and Chest Congestion Childrens 69842-0657-08 CVS 1 kit — — FDA listed —
Kids Daytime Cough and Nighttime Cough combo pack 69676-0107-03 Genexa 2 bottles — — 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

🏛️
2020
On the market since
Apr 2020
📍
2026
Currently FDA-listed
6 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.

What it looks like

Color purple / red
FlavorFruit Punch
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 Dextromethorphan / Guaifenesin 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.

From the label’s inactive-ingredient sectionInactive ingredients for Day Time Wal-Tussin DM   anhydrous citric acid, carboxymethylcellulose sodium, edetate disodium, FD &C Blue No. 1, FD&C Red No. 40, natural and artificial flavors, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum Inactive ingredients for Night Time Wal-Tussin DM   anhydrous citric acid, FD&C Red No. 40, natural and artificial flavors, glycerin, lactic acid, potassium sorbate, 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

LabelerWALGREEN CO
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code00363
First marketedApr 2020
Product typeHuman Otc Drug
Portfolio6 products on file

More NDCs from WALGREEN CO labeler code 00363

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 📄 Do Not Use 📄 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 72 words ▾

Uses DAYTIME temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes NIGHTTIME temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itching of the nose or throat itchy, watery eyes

⏱️ Dosage and Administration 132 words ▾

Directions Daytime Wal-Tussin ® DM do not take more than 6 doses in any 24-hour period measure only with dosing cup provided. keep dosing cup with product mL= milliliter age dose Children under 4 years Do not use Children 4 to under 6 years 5 mL every 4 hours Children 6 to under 12 years 10 mL every 4 hours Adults and children 12 years and older 20 mL every 4 hours Nighttime Wal-Tussin ® DM do not take more than 4 doses in any 24-hour period measure only with dosing cup provided. keep dosing cup with product mL= milliliter age dose Children under 6 years Do not use Children 6 to under 12 years 10 mL every 6 hours Adults and children 12 years and older 20 mL every 6 hours

⚠️ Warnings ~2 min read ▾

Warnings Do not us DAYTIME 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 prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. NIGHTTIME 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 prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have DAYTIME cough that occurs with too much phlegm (mucus) cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema NIGHTTIME trouble urinating due to an enlarges prostate gland glaucoma a cough that occurs with too much phlegm (mucus) a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema Ask a doctor or pharmacist before use if you are NIGHTTIME taking sedatives or tranquilizers.

When using this product NIGHTTIME do not use more than directed. marked drowsiness may occur avoid alcoholic drinks 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 cough last more than 7 days, comes back or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. NIGHTTIME cough last more than 7 days, comes back or is accompanied by fever, rash, or persistent headache.

These could be signs of a serious condition. If pregnant or breast-feeding, DAYTIME ask a health professional before use. NIGHTTIME ask a health professional before use Keep out of reach of children.

DAYTIME In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. NIGHTTIME In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away

📦 Storage and Handling 66 words ▾

Other information DAYTIME Wal-Tussin DM each 20 mL contains: sodium 11 mg store at room temperature. Do not refrigerate contain low sodium do not use if printed seal under cap is torn or missing Nighttime Wal-Tussin DM each 10 mL contains: sodium 6 mg store at room temperature. Do not refrigerate contain low sodium do not use if printed seal under cap is torn or missing

🧪 Active Ingredient 35 words ▾

Active ingredients Day Time (in each 20 mL) Dextromethorphan HBr USP 20 mg Guaifenesin. USP 200 mg

Active ingredients for Nighttime (in each 10 mL) Chlorpheniramine maleate, USP 2 mg Dextromethorphan HBr USP 15 mg

🧪 Inactive Ingredients 75 words ▾

Inactive ingredients Inactive ingredients for Day Time Wal-Tussin DM anhydrous citric acid, carboxymethylcellulose sodium, edetate disodium, FD &C Blue No. 1, FD&C Red No. 40, natural and artificial flavors, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum Inactive ingredients for Night Time Wal-Tussin DM anhydrous citric acid, FD&C Red No.

40, natural and artificial flavors, glycerin, lactic acid, potassium sorbate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose

🎯 Purpose 18 words ▾

Purposes for Daytime Wal-Tussin ® DM Cough suppressant Expectorant

Purpose for Nighttime Wal-Tussin ® DM Antihistamine Cough suppressant

📄 Do Not Use 119 words ▾

Do not us DAYTIME 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 prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. NIGHTTIME 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 prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

📄 Ask a Doctor Before Use If 70 words ▾

Ask a doctor before use if you have DAYTIME cough that occurs with too much phlegm (mucus) cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema NIGHTTIME trouble urinating due to an enlarges prostate gland glaucoma a cough that occurs with too much phlegm (mucus) a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema

📄 Ask a Doctor or Pharmacist Before Use If 15 words ▾

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

📄 When Using This Product 41 words ▾

When using this product NIGHTTIME do not use more than directed. marked drowsiness may occur avoid alcoholic drinks 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 77 words ▾

Stop use and ask a doctor if DAYTIME cough last more than 7 days, comes back or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. NIGHTTIME cough last more than 7 days, comes back or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. If pregnant or breast-feeding, DAYTIME ask a health professional before use. NIGHTTIME ask a health professional before use

🤰 If Pregnant or Breast-Feeding 18 words ▾

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

📄 Keep Out of Reach of Children 40 words ▾

Keep out of reach of children. DAYTIME In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. NIGHTTIME In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away

📄 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 Children's Robitussin ® Cough & Chest Congestion DM* & Nighttime Cough DM Long-Active active ingredients †† Children's Cough & Chest Congestions DM Wal-Tussin ® DM DEXTROMETHORPHAN HBr, USP 20 mg/ 20 mL COUGH SUPPRESSANT GUAIFENESIN, USP 200 mg EXPECTORANT DAYTIME NON-DROWSY Relieves cough, chest congestion & mucus 4 YEARS & OVER GRAPE FLAVOR Naturally and Artificially Flavored Dosage cup included 2 - 4 FL OZ (118 mL) BOTTLES / TOTAL – 8 FL OZ (236 mL) †† This product is not manufactured or distributed by Pfizer, the distributor of Children’s Robitussin ® Cough & Chest Congestion DM.

Children's Nighttime Cough DM Wal-Tussin ® DM CHLORPHENIRAMINE MALEATE, USP 2 mg / 10 mL ANTIHISTAMINE DEXTROMETHORPHAN HBr, USP 15 mg / 10 mL COUGH SUPPRESSANT NIGHTTIME Relieves cough & runny nose Alcohol free 6 YEARS & OLDER Fruit Punch Flavor Naturally and Artificially Flavored Dosage cup included 2 - 4 FL OZ (118 mL) BOTTLES TOTAL – 8 FL OZ (236 mL) †† This product is not manufactured or distributed by Pfizer, the distributor of Children’s Robitussin ® Nighttime Cough DM Long-Acting. Walgreens PHARMACIST RECOMMENDED TAMPER EVIDENT: DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING DISTRIBUTED BY: WALGREENS CO.

200 WILMOT RD. DEERFIELD, IL 60015 Walgreens 10% SATISFACTION GUARANTEED walgreens.com ©2020 Walgreen Co. Walgreens Childrens Day Time & Nighttime Wal Tussin DM Twin Pack

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 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 ✓ 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 WALGREEN CO. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
WALGREEN CO 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.
← 00363-7560-04 · WALGREENS 00363-7590-30 · WALGREENS →
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.