Home › NDC Lookup › Ingredients › Dextromethorphan Hbr, Guaifenesin, Chlor... › 69842-0657-08
📦image loading
(from DailyMed)

Daytime and Nighttime Cough and Chest Congestion Childrens Dextromethorphan HBr, Guaifenesin, Chlorpheniramine maleate Kit — NDC 69842-657-08 (Billing 69842-0657-08)

by CVS Pharmacy · 1 KIT in 1 KIT * 118 mL in 1 BOTTLE * 118 mL in 1 BOTTLE

This is a package of Daytime and Nighttime Cough and Chest Congestion Childrens Dextromethorphan HBr, Guaifenesin, Chlorpheniramine maleate Kit from CVS Pharmacy, marketed since Feb 2019 and currently FDA-listed. It is this product's only package size.

NDC 69842-0657-08
🏷️ FDA NDC (as labeled) 69842-657-08 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Sep 3, 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 69842-657-08 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69842 labeler · 657 product · 08 package
Package marketed since
Feb 19, 2019
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0050428548080
FDA record last changed
Sep 3, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69842-657-08
Product NDC 69842-657
11-digit billing NDC 69842065708
RxCUI 1020138, 1111440, 2119625
UPC 0050428548080
Application # M012
SPL Set ID 347f1731-5b85-4220-ae2b-9497a3afa4ed
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-02-19
Dosage form KIT
Quick answers
  • RxCUI (RxNorm): 1020138
Why two NDCs? The FDA registers this code as 69842-657-08 — 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 → 69842-0657-08. 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 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.

Clinical

📗 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
69842-0657-08 You're viewing this Main listing 1 KIT in 1 KIT * 118 mL in 1 BOTTLE * 118 mL in 1 BOTTLE 2019-02-19 — 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 PACK 00363-7570-08 WALGREEN 1 kit — — FDA listed —
Daytime and Nighttime Cough and Chest Congestion Childrensthis 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

🏛️
2019
On the market since
Feb 2019
📍
2026
Currently FDA-listed
7 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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

LabelerCVS Pharmacy
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code69842
First marketedFeb 2019
Product typeHuman Otc Drug
Portfolio550 products on file

More NDCs from CVS Pharmacy labeler code 69842

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 80 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 134 words ▾

Directions DAYTIME • measure only with dosing cup provided. • keep dosing cup with product • mL= milliliter • do not take more than 6 doses in any 24-hour period 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 • measure only with dosing cup provided. • keep dosing cup with product • mL= milliliter • do not take more than 4 doses in any 24-hour period 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 70 words ▾

Other information DAYTIME • each 5 mL contains: sodium 3 mg • store at room temperature. Do not refrigerate • contain low sodium • do not use if printed seal under cap is torn or missing NIGHTTIME • each 10 mL contains: sodium 3 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 5 mL) Dextromethorphan HBr USP 5 mg Guaifenesin. USP 100 mg

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

🧪 Inactive Ingredients 64 words ▾

Inactive ingredients Inactive ingredients for Day Time anhydrous citric acid, edetate disodium, FD&C Blue # 1, FD&C Red # 40, natural and artificial flavors, potassium citrate, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum Inactive ingredients for Night Time anhydrous citric acid, FD&C Red # 40, natural and artificial flavors, potassium sorbate, potassium citrate, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose

🎯 Purpose 14 words ▾

Purposes for Day Time Cough suppressant Expectorant

Purpose for Night Time Antihistamine Cough suppressant

📄 Do Not Use 122 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 76 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 47 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 79 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 the active ingredients in Children's Robitussin ® Cough & Chest Congestion DM* Non-Drowsy Children's Cough & Chest Congestions DM Each 5 mL dose of oral solution contains: DEXTROMETHORPHAN HBr, USP 5 mg Cough suppressant GUAIFENESIN, USP 100 mg Expectorant Relieves • Chest congestion/mucus • Cough For Ages 4 and over Grape Flavor Naturally and Artificially Flavored Dosage cup included TWO 4 FL OZ (118 mL) BOTTLES TOTAL – 8 FL OZ (236 mL) Compare to the active ingredients in Children's Robitussin ® Nighttime Cough DM* NDC# 69842-657-08 Children's Nighttime Cough DM Each 10 mL dose of oral solution contains: CHLORPHENIRAMINE MALEATE, USP 2 mg Antihistamine DEXTROMETHORPHAN HBr, USP 15 mg Cough suppressant Relieves • Cough up to 8 hours • Runny nose Alcohol free For Ages 6 & over Fruit Punch Flavor Naturally and Artificially Flavored Dosage cup included TWO 4 FL OZ (118 mL) BOTTLES TOTAL – 8 FL OZ (236 mL) * This product is not manufactured or distributed by Pfizer, owner of the registered trademarks Children’s Robitussin ® Cough + Chest Congestion DM and Children’s Robitussin ® Nighttime Cough DM.

Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895 ©2018 CVS/pharmacy CVS.com ® 1-800-SHOP CVS V-12431 CVS ® Quality Money Back Guarantee CVS Health Children's Daytime & Nighttime Cough & Chest Congestion DM

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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 CVS Pharmacy. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
CVS Pharmacy 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.
← 69842-0652-14 · CVS 69842-0659-63 · CVS →
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.