ultra sleep aid Doxylamine Succinate 25 mg Tablet, 24-count
by Walgreen Company · 24 BLISTER PACK in 1 CARTON (0363-8011-62) / 1 TABLET in 1 BLISTER PACK
NDC 00363-8011-62
🏷️ FDA NDC (as labeled)
0363-8011-62
billing pads the labeler segment with a zero
OTC
Generic
On market
Non-controlled
🗂️ Data synced Sep 3, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
0363-8011-62
Product NDC
0363-8011
11-digit billing NDC
00363801162
RxCUI
1101446
UNII
V9BI9B5YI2
Application #
ANDA040167
SPL Set ID
90a5986d-2555-4c2d-8e41-16537ff1aa36
Established class (EPC)
Antihistamine
Mechanism of action
Histamine Receptor Antagonists
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2025-02-14
Route
ORAL
Dosage form
TABLET
Substance
DOXYLAMINE SUCCINATE
Why two NDCs?
The FDA registers this code as 0363-8011-62 — 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 → 00363-8011-62. 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 Antihistamine class.
Pharmacologic class
Antihistamine
Drug family (ATC)
Aminoalkyl ethers
How it works
Histamine Receptor Antagonists
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
🏭 Manufacturer & labeler
LabelerWalgreen Company
Application holderL PERRIGO CO
FDA applicationANDA040167 (ANDA)
Labeler code00363
First marketedFeb 2025
Product typeHuman Otc Drug
Portfolio468 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
📗 Our plain-language guide HelloPharmacist
- It depends on the product you have. If you picked up a sleep-aid tablet — like Nighttime Sleep Aid or berkley and jensen sleep aid — it's meant to help you fall asleep more easily....
- For sleep-aid tablets, the directions say to take one tablet about 30 minutes before you plan to go to bed, and only once per night. It's important that you have a full night's sle...
- How do I take the sleep-aid tablet — can I take it earlier in the evening?
- No — please avoid alcohol entirely while you're using doxylamine. Alcohol and doxylamine both cause drowsiness, and combining them can make the sedation much stronger than you expe...
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Doxylamine Succinate — tap one for details:
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
💬 Questions about Doxylamine Succinate?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
Blue
ShapeOval
ImprintL441
Size1 mm
ScoringScored — splits in 2
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
🧪 Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII L11K75P92J
A mineral salt made from calcium and phosphate. It acts as a filler and binder in tablets to add bulk and help hold the medicine together in solid form.
-
UNII O7TSZ97GEP
A mineral compound that serves as a filler and binding agent in tablets and capsules. It adds bulk to the medicine and helps hold ingredients together during manufacturing.
-
UNII J9EQA3S2JM
FD&C Blue No. 1 Aluminum Lake is a blue colorant made by combining FD&C Blue No. 1 dye with aluminum salts. It is used to color tablets, capsules, and other medicines for easy identification and appearance.
-
UNII 70097M6I30
Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
-
UNII OP1R32D61U
Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
-
UNII H8AV0SQX4D
A modified starch derived from potato or corn starch. It absorbs water quickly and helps tablets or capsules break apart and dissolve in the stomach, acting as a disintegrant to ensure the medicine releases its active ingredients properly.
6 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesanhydrous dibasic calcium phosphate, dibasic calcium phosphate dihydrate, FD&C blue no. 1 aluminum lake, magnesium stearate, microcrystalline cellulose, sodium starch glycolate
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed —
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
💲 Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per each | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Good sense sleep aid 25 mg 00113-0441-64 | L. | 32 tablets | $0.116 | — | Availability likely | — |
| good sense sleep aid ultra 25 mg 00113-4032-62 | L. | 24 tablets | $0.116 | — | Availability likely | — |
| Nighttime Sleep Aid 25 mg 46122-0788-15 | Amerisource | 32 tablets | $0.116 | — | Availability likely | — |
| Sleep-Aid 25 mg 70000-0567-01 | Cardinal | 48 tablets | $0.116 | — | Availability likely | — |
| Sleep Aid 25 mg 70677-1129-01 | Strategic | 32 tablets | $0.116 | — | Availability likely | — |
| good sense sleep aid ultra 25 mg 00113-6044-67 | L. | 48 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 00363-0386-12 | Walgreen | 100 tablets | — | — | FDA listed | — |
| sleep aid 25 mg 00363-3462-80 | Walgreen | 96 tablets | — | — | FDA listed | — |
| ultra sleep aid 25 mgthis 00363-8011-62 | Walgreen | 24 tablets | — | — | FDA listed | — |
| up and up nighttime sleep aid 25 mg 11673-0171-01 | Target | 96 tablets | — | — | FDA listed | — |
| sleep aid 25 mg 11822-0441-00 | Rite | 48 tablets | — | — | FDA listed | — |
| sleep aid 25 mg 11822-3000-00 | Rite | 24 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid 25 mg 21130-0986-27 | Better | 32 tablets | — | — | FDA listed | — |
| Nighttime Sleep-Aid 25 mg 30142-0366-27 | Kroger | 32 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 30142-0386-27 | Kroger | 32 tablets | — | — | FDA listed | — |
| TopCare Sleep Aid 25 mg 36800-0441-64 | Topco | 32 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid 25 mg 37808-0886-27 | H | 32 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 41163-0986-22 | United | 48 tablets | — | — | FDA listed | — |
| Unisom SleepTabs 25 mg 41167-0063-05 | Chattem, | 16 tablets | — | — | FDA listed | — |
| Unisom SleepTabs 25 mg 41167-0608-00 | Chattem, | 16 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 41250-0441-01 | Meijer | 96 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 41250-0986-22 | Meijer | 48 tablets | — | — | FDA listed | — |
| CareOne Nighttime Sleep Aid 25 mg 41520-0634-64 | American | 32 tablets | — | — | FDA listed | — |
| nighttime sleep aid 25 mg 42507-0033-64 | HyVee | 32 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 49035-0968-27 | Wal-Mart | 32 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid 25 mg 50844-0260-21 | L.N.K. | 16 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid 25 mg 50844-0386-19 | L.N.K. | 8 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 51316-0368-22 | CVS | 48 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 55301-0986-27 | ARMY | 32 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid 25 mg 55319-0439-16 | Family | 16 tablets | — | — | FDA listed | — |
| dg health sleep aid 25 mg 55910-0909-53 | Dolgencorp | 12 tablets | — | — | FDA listed | — |
| sleep aid 25 mg 56062-0441-01 | Publix | 96 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid 25 mg 59779-0441-01 | CVS | 96 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 63981-0986-96 | COSTCO | 96 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid, 24-7 Life by 7-Eleven 25 mg 66715-5642-04 | Lil' | 16 tablets | — | — | FDA listed | — |
| ZzzQuil ULTRA, Travel BASIX 25 mg 66715-6451-03 | Lil' | 3 tablets | — | — | FDA listed | — |
| ZzzQuil ULTRA, Lil Drug Store 25 mg 66715-9751-02 | Lil' | 2 tablets | — | — | FDA listed | — |
| berkley and jensen sleep aid 25 mg 68391-0441-02 | BJWC | 192 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid 25 mg 69168-0439-06 | Allegiant | 120 tablets | — | — | FDA listed | — |
| Vicks ZzzQuil Ultra 25 mg 69423-0902-12 | The | 12 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid 25 mg 69842-0386-22 | CVS | 48 tablets | — | — | FDA listed | — |
| Basic Care Sleep Aid 25 mg 72288-0441-01 | Amazon.com | 96 tablets | — | — | FDA listed | — |
| SLEEP AID 25mg 25 mg 73581-0205-02 | YYBA | 200 tablets | — | — | FDA listed | — |
| Topcare Sleep Aid 25 mg 76162-0159-62 | Topco | 24 tablets | — | — | FDA listed | — |
| topcare sleep aid 25 mg 76162-0603-67 | Topco | 48 tablets | — | — | FDA listed | — |
| sleep aid ultra 25 mg 79481-0096-00 | Meijer, | 24 tablets | — | — | FDA listed | — |
| Night Time Sleep Aid 25 mg 80513-0371-25 | Advanced | 225 tablets | — | — | FDA listed | — |
| Nighttime Sleep Aid 25 mg 85828-0439-38 | Grocery | 32 tablets | — | — | FDA listed | — |
| Nocto Sleep Aid 25 mg 27854-0375-01 | Belmora | 24 tablets | — | — | FDA listed | — |
| Sleep Aid 25 mg 72288-0432-01 | Amazon.com | 96 tablets | — | — | FDA listed | — |
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
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
🏛️
2025
On the market since
Feb 2025
📍
2026
Currently FDA-listed
1 year listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug
This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Doxylamine Succinate — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 33%
Female · 67%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 00363-8011-62 You're viewing this | 24 BLISTER PACK in 1 CARTON (0363-8011-62) / 1 TABLET in 1 BLISTER PACK | 2025-02-14 | Active |
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
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 0363-8011-62, 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: 00363-8011-62, written without dashes as 00363801162. 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 00363-8011-62, the first segment (00363) is the labeler code FDA assigned to Walgreen Company; the middle segment (8011) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (62) 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 Walgreen Company. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Walgreen Company 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
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Use • helps to reduce difficulty in falling asleep
⏱️ Dosage and Administration ▾
Directions • adults and children 12 years of age and over: take one tablet 30 minutes before going to bed; take once daily or as directed by a doctor • children under 12 years of age: do not use
⚠️ Warnings ▾
Warnings Do not use • in children under 12 years of age • with any other product containing doxylamine • unless you have time for a full night’s sleep Ask a doctor before use if you have • a breathing problem such as emphysema or chronic bronchitis • glaucoma • trouble urinating due to an enlarged prostate gland Ask a doctor or pharmacist before use if you are taking • a sedative or any other sleep-aid • tranquilizers • any other antihistamines • any other drugs When using this product • avoid alcoholic beverages • do not drive a motor vehicle or operate machinery • take only at bedtime Stop use and ask a doctor if • sleeplessness persists continuously for more than two weeks.
Insomnia may be a symptom of serious underlying medical illness. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
🧪 Active Ingredient ▾
Active ingredient (in each tablet) Doxylamine succinate 25 mg
🧪 Inactive Ingredients ▾
Inactive ingredients anhydrous dibasic calcium phosphate, dibasic calcium phosphate dihydrate, FD&C blue no. 1 aluminum lake, magnesium stearate, microcrystalline cellulose, sodium starch glycolate
🎯 Purpose ▾
Purpose Nighttime sleep-aid
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.