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Daytime Nighttime Chewable Dextromethorphan HBr Doxylamine Succinate Kit — NDC 00363-9393-32 package photo

Daytime Nighttime Chewable Dextromethorphan HBr Doxylamine Succinate Kit

by Walgreens · 1 KIT in 1 KIT (0363-9393-32) * 16 CHEWABLE GEL in 1 BOTTLE, PLASTIC (0363-9358-16) * 16 CHEWABLE GEL in 1 BOTTLE, PLASTIC (0363-9360-16)
NDC 00363-9393-32
🏷️ FDA NDC (as labeled) 0363-9393-32 billing pads the labeler 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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 0363-9393-32
Product NDC 0363-9393
11-digit billing NDC 00363939332
RxCUI 2683423, 2683424, 2683425
UPC 0311917070957
Application # M012
SPL Set ID 9ddc0aa7-e7b8-41c5-a2b4-fece0c2e26c6
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-30
Dosage form KIT
Why two NDCs? The FDA registers this code as 0363-9393-32 — 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 → 00363-9393-32. 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 Uncompetitive N-methyl-D-aspartate Receptor Antagonist class.

Pharmacologic class Uncompetitive N-methyl-D-aspartate Receptor Antagonist, Sigma-1 Agonist
Drug family (ATC) Other antidepressants, Opium alkaloids and derivatives
How it works Uncompetitive NMDA Receptor Antagonists, Sigma-1 Receptor Agonists
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

LabelerWalgreens
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code00363
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio339 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

📖 About the active ingredient: Dextromethorphan HBr Doxylamine Succinate MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.

Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.

Read the full MedlinePlus article ↗
🧪 What is this product?

This is an over-the-counter chewable kit containing dextromethorphan and doxylamine, two ingredients commonly found in cold and cough products. Dextromethorphan is a cough suppressant typically used to reduce coughing, while doxylamine is an antihistamine commonly used to relieve sneezing, runny nose, and other allergy-like symptoms. The kit format offers daytime and nighttime formulations, which generally differ in drowsiness-causing ingredients to match usage timing. This product is marketed under FDA's OTC monograph rules for cough-cold category drugs.

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.

💊 What it looks like

Color red / purple
ShapeRound
ImprintP
ScoringNot scored
FlavorBerry
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.

From the label’s inactive-ingredient sectionDAYTIME  ammonium glycyrrhizate, anhydrous citric acid, corn syrup, FD&C red # 40, flavors, glycerin, glycyrrhizin, malic acid, maltodextrin, medium-chain triglycerides, pectin, propylene glycol, purified water, sorbitol solution, sucralose, sucrose, trisodium citrate dihydrate  NIGHTTIME  alcohol, ammonium glycyrrhizate, anhydrous citric acid, corn syrup, FD&C blue #1, FD&C Red #40, flavors, glycerin, glycyrrhizin, malic acid, maltodextrin, pectin, propylene glycol, purified water, sucralose, sucrose, trisodium citrate dihydrate 

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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Daytime Nighttime Chewablethis 00363-9393-32 Walgreens 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

🏛️
2026
On the market since
Apr 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
00363-9393-32 You're viewing this 1 KIT in 1 KIT (0363-9393-32) * 16 CHEWABLE GEL in 1 BOTTLE, PLASTIC (0363-9358-16) * 16 CHEWABLE GEL in 1 BOTTLE, PLASTIC (0363-9360-16) 2026-04-30 Active

🧭 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 FDA registers it as 0363-9393-32, 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: 00363-9393-32, written without dashes as 00363939332. 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 00363-9393-32, the first segment (00363) is the labeler code FDA assigned to Walgreens; the middle segment (9393) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (32) 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 Walgreens. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Walgreens 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 68 words ▾

Uses DAYTIME temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold NIGHTTIME temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold controls cough to help you get to sleep temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itching of the nose or throat sneezing itchy, watery eyes

⏱️ Dosage and Administration 76 words ▾

Directions DAYTIME / NIGHTTIME take every 4 hours or as directed by a doctor chew thoroughly before swallowing adults and children 12 years of age and over: 2 chewable gels every 4 hours, not to exceed 12 chewable gels in any 24-hour period children 6 to under 12 years of age: 1 chewable gel every 4 hours, not to exceed 6 chewable gels in any 24-hour period children under 6 years of age: do not use

⚠️ Warnings ~2 min read ▾

Warnings Do not use 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 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) persistent or chronic cough such as occurs with smoking, asthma or emphysema NIGHTTIME glaucoma 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 trouble urinating due to enlarged prostate gland Ask a doctor or pharmacist before use if you are NIGHTTIME taking sedatives or tranquilizers When using this product DAYTIME do not use more than directed.

NIGHTTIME do not exceed recommended dosage excitability may occur, especially in children marked drowsiness may occur avoid alcoholic drinks alcohol, sedatives and tranquilizers may increase drowsiness use caution when driving a motor vehicle or operating machinery Stop use and ask a doctor if DAYTIME cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition. NIGHTTIME cough lasts 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 NIGHTTIME ask a health professional before use. Keep out of reach of children. DAYTIME / NIGHTTIME In case of overdose, get medical help or contact a Poison Control Center(1-800-222-1222) right away.

📦 Storage and Handling 32 words ▾

Other information DAYTIME each chewable gel contains: sodium 8 mg store between 20-25ºC (68-77º). Do not refrigerate NIGHTTIME each chewable gel contains sodium 6 mg store between 20-25ºC (68-77ºF). Do not refrigerate

🧪 Active Ingredient 27 words ▾

Active ingredient (in each chewable gel) Daytime Dextromethorphan HBr 10 mg

Active ingredients for (in each chewable gel) NIGHTTIME Dextromethorphan HBr 10 mg Doxylamine Succinate 6.25 mg

🧪 Inactive Ingredients 65 words ▾

Inactive ingredient DAYTIME ammonium glycyrrhizate, anhydrous citric acid, corn syrup, FD&C red # 40, flavors, glycerin, glycyrrhizin, malic acid, maltodextrin, medium-chain triglycerides, pectin, propylene glycol, purified water, sorbitol solution, sucralose, sucrose, trisodium citrate dihydrate NIGHTTIME alcohol, ammonium glycyrrhizate, anhydrous citric acid, corn syrup, FD&C blue #1, FD&C Red #40, flavors, glycerin, glycyrrhizin, malic acid, maltodextrin, pectin, propylene glycol, purified water, sucralose, sucrose, trisodium citrate dihydrate

🎯 Purpose 11 words ▾

Purpose for Daytime Cough suppressant

Purposes for Nighttime Cough suppressant Antihistamine

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 00363-9390-10 · Walgreen 00363-9410-97 · WALGREEN →
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.