Walgreens diphenhydramine hydrochloride, ibuprofen, hydrocortisone, bacitracin zinc, neomycin sulfate, polymyxin-B sulfate, lidocaine HCL, benzalkonium chloride, isopropyl alcohol, ethyl alcohol Kit — NDC 00363-1500-01 package photo

Walgreens diphenhydramine hydrochloride, ibuprofen, hydrocortisone, bacitracin zinc, neomycin sulfate, polymyxin-B sulfate, lidocaine HCL, benzalkonium chloride, isopropyl alcohol, ethyl alcohol Kit

by Walgreen Co. · 1 KIT in 1 CASE (0363-1500-01) * .9 g in 1 POUCH (61010-5600-1) * .34 g in 1 POUCH (51142-445-21) * .9 g in 1 POUCH (61010-5800-1) * 2 TABLET, COATED in 1 PACKET (47682-718-99) * .0019 L in 1 PACKET (61010-2017-0) * 1 TABLET, FILM COATED in 1
NDC 00363-1500-01
🏷️ FDA NDC (as labeled) 0363-1500-01 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 →

🆔 Identity & classification

FDA NDC (as labeled) 0363-1500-01
Product NDC 0363-1500
11-digit billing NDC 00363150001
Application # 505G(a)(3)
SPL Set ID 5630f48b-404c-b847-e063-6394a90a8d8e
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-07-17
Route ORAL
Dosage form KIT
Why two NDCs? The FDA registers this code as 0363-1500-01 — 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 → 00363-1500-01. 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 Corticosteroid class.

Pharmacologic class Corticosteroid
Drug family (ATC) Corticosteroids, moderately potent (group II), Corticosteroids, potent (group III), Corticosteroids for local oral treatment
How it works Corticosteroid Hormone 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

LabelerWalgreen Co.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code00363
First marketedJul 2024
Product typeHuman Otc Drug
Portfolio132 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

🧪 What is this product?

This is an over-the-counter oral medication kit containing multiple active ingredients. Diphenhydramine hydrochloride is an antihistamine typically used to relieve allergy and cold symptoms. Ibuprofen is a pain reliever and fever reducer. Hydrocortisone is a mild steroid typically used to reduce inflammation and itching. The kit also includes topical antibiotic and antiseptic ingredients (bacitracin zinc, neomycin sulfate, polymyxin-B sulfate, lidocaine, benzalkonium chloride, and alcohol) that are commonly found in first-aid products to help prevent infection and numb minor pain.

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 pink / white / red
ShapeRound
ImprintG;2
Size1 mm
ScoringNot scored
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 sectioncroscarmellose sodium, D&C red #27 aluminum lake, hypromellose, lactose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, titanium dioxide aloe vera, fragrance, purified water, triethanolamine petrolatum aloe vera, emulsifying wax, ethyl alcohol, methylparaben, mineral oil, paraffin, propylparaben, purified water, white petrolatum, white wax purified water emulsifying wax, ethanol, methylparaben, mineral oil, paraffin, petrolatum, propylparaben, purified water, white wax colloidal silicon dioxide, corn starch, iron oxide red, polyethylene glycol, povidone (K30), sodium starch glycolate, stearic acid, talc, titanium dioxide

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
Care Science 51142-0005-01 ASO 2 tablets FDA listed
Walgreensthis 00363-1500-01 Walgreen 2 tablets 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
Jul 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
00363-1500-01 You're viewing this 1 KIT in 1 CASE (0363-1500-01) * .9 g in 1 POUCH (61010-5600-1) * .34 g in 1 POUCH (51142-445-21) * .9 g in 1 POUCH (61010-5800-1) * 2 TABLET, COATED in 1 PACKET (47682-718-99) * .0019 L in 1 PACKET (61010-2017-0) * 1 TABLET, FILM COATED in 1 2024-07-17 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 0363-1500-01, 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: 00363-1500-01, written without dashes as 00363150001. 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 00363-1500-01, the first segment (00363) is the labeler code FDA assigned to Walgreen Co.; the middle segment (1500) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 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.

📄 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 199 words

Uses – Diphen Allergy Caplet Temporarily relieves these symptoms due to hay fever or other respiratory allergies runny nose sneezing itching of the nose or throat itchy, watery eyes Temporarily relieves these symptoms due to the common cold runny nose sneezing

Uses – Antiseptic Wipes Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water

Uses – Triple Antibiotic Ointment first aid to help prevent infection in minor cuts, scrapes, and burns

Uses – First Aid and Burn Cream temporary relief of pain associated with minor burns helps protect against harmful bacteria

Uses – Alcohol Prep Pads For preparation of the skin prior to an injection

Uses – Hydrocortisone Cream for the temporary relief of itching associated with minor skin irritations, inflammation and rashes due to eczema, insect bites, poison ivy, poison oak, poison sumac, soaps, detergents, cosmetics, jewelry, seborrheic dermatitis, psoriasis and scrapes other uses of this product should be only under the advice and supervision of a doctor

Uses – Ibuprofen Temporarily relieves minor aches and pains associated with • headache • toothache • backache • menstrual cramps • common cold • muscular aches • minor arthritis pain Temporarily reduces fever.

⏱️ Dosage and Administration ~1 min read

Directions – Diphen Allergy Caplet take every 4-6 hours, or as directed by a doctor do not take more than 6 times in 24 hours Adults and children: (12 years and over) 1 to 2 caplets Children under 12 years: do not use

Directions – Antiseptic Wipes tear open packet, remove towelette unfold and use as a washcloth supervise children under 6 years of age

Directions – Triple Antibiotic Ointment Clean the affected area Apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily May be covered with a sterile bandage

Directions – First Aid and Burn Cream clean affected area apply small amount not more than 3 times daily children under 2: consult a doctor

Directions – Alcohol Prep Pads wipe injection area and discard

Directions – Hydrocortisone Cream for adults and children 2 years of age and older: apply to affected area 3 to 4 times daily children under 2 years of age: do not use, consult a doctor adults for external anal itching when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly or by patting or blotting with an appropriate cleansing pad gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product children under 12 years of age: for external anal itching, consult a doctor

Directions – Ibuprofen • do not use more than directed • the smallest effective dose should be used • do not take longer than 10 days, unless directed by a doctor (see Warnings) Adults and children: (12 years and older) Take 1 tablet every 4 to 6 hours while symptoms persist. If pain or fever does not respond to 1 tablet, 2 tablets may be used. Do not exceed 6 tablets in 24 hours, unless directed by a doctor. Children under 12 years: Ask a doctor

⚠️ Warnings ~3 min read

Warnings – Diphen Allergy Caplet . Do not use – Diphen Allergy Caplet to make a child sleepy with any other product containing diphenhydramine, even one that is used on skin. Ask a doctor before use if you have – Diphen Allergy Caplet a breathing problem such as emphysema or chronic bronchitis difficulty in urinating due to enlargement of the prostate gland glaucoma Ask a doctor or pharmacist before use if you are – Diphen Allergy Caplet taking sedatives or tranquilizers When using this product – Diphen Allergy Caplet marked drowsiness may occur avoid alcoholic beverages alcohol, sedatives and tranquilizers may increase the drowsiness effect use caution when driving a motor vehicle or operating machinery excitability may occur, especially in children If pregnant or breast-feeding, – Diphen Allergy Caplet ask a health care professional before use.

Keep out of reach of children. – Diphen Allergy Caplet In case of overdose, contact a physician or poison control center immediately

Warnings – Antiseptic Wipes For external use only Flammable: keep away from fire or flame Do not use – Antiseptic Wipes in the eyes. If this happens, rinse thoroughly with water. Stop use and ask a doctor – Antiseptic Wipes if irritation or redness develop and persist for more than 72 hours Keep out of reach of children – Antiseptic Wipes If swallowed get medical help or contact a Poison Control Center right away

Warnings – Triple Antibiotic Ointment For external use only Do not use – Triple Antibiotic Ointment internally in eyes over large areas of the body for more than 1 week unless directed by a doctor if you are allergic to any of the ingredients Ask a doctor before use - Triple Antibiotic Ointment in case of deep or puncture wounds, animal bites, or serious burns Stop use and ask a doctor if – Triple Antibiotic Ointment a rash or allergic reaction develops the condition persists or gets worse Keep out of reach of children – Triple Antibiotic Ointment In case of accidental ingestion, seek professional assistance or contact a poison control center immediately.

Warnings – First Aid and Burn Crean For external use only Do not use – First Aid and Burn Crean in eyes in large quantities over raw or blistered areas, or on deep puncture wounds, animal bites, serious burns for more than one week unless directed by a doctor Stop use, ask a doctor – First Aid and Burn Crean condition worsens or if symptoms persist for more than 7 days or clear up and occurs again within a few days Keep out of reach of children. – First Aid and Burn Cream If ingested, contact a Poison Control Center right away

Warnings – Alcohol Prep Pads For external use only Flammable, keep away from fire or flame Do not use – Alcohol Prep Pads with electrocautery procedures in the eyes. If contact occurs, flush eyes with water. Stop use if – Alcohol Prep Pads irritation and redness develop.

If condition continues, consult your health care practitioner Keep out of reach of children. – Alcohol Prep Pads If swallowed get medical help or contact a Poison Control Center right away.

Warnings – Hydrocortisone Cream For external use only Do not use – Hydrocortisone Cream for the treatment of diaper rash in eyes for feminine itching if condition worsens or lasts more than 7 days, or clears up and occurs again within a few days with any other Hydrocortisone product unless you have consulted a doctor Keep out of reach of children. – Hydrocortisone Cream If swallowed, get medical help or contact a Poison Control Center right away.

Warnings – Ibuprofen Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: • hives • skin reddening • asthma (wheezing) • facial swelling • rash • shock • blisters If an allergic reaction occurs, stop use and seek medical help right away. Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding.

The chance is higher if you: • are age 60 or older • have had st…

🧪 Active Ingredient 93 words

Active ingredient (in each caplet) – Diphen Allergy Caplet Diphenhydramine Hydrochloride 25 mg

Active ingredients – Antiseptic Wipes Ethyl Alcohol 66.5%

Active Ingredient (in each gram) – Triple Antibiotic Ointment Bacitracin Zinc (400 units Bacitracin) Neomycin Sulfate (3.5 mg Neomycin) Polymyxin B Sulfate (Polymyxin B 5000 units)

Active Ingredient – First Aid and Burn Cream Benzalkonium Chloride 0.13% Lidocaine HCl 0.5%

Active ingredient – Alcohol Prep Pads Isopropyl Alcohol 70%

Active ingredient – Hydrocortisone Cream Hydrocortisone 1.0%

Active ingredient ( in each tablet ) – Ibuprofen Ibuprofen 200 mg (NSAID*) *nonsteroidal anti-inflammatory drug

🧪 Inactive Ingredients 118 words

Inactive Ingredients – Diphen Allergy Caplet croscarmellose sodium, D&C red #27 aluminum lake, hypromellose, lactose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, titanium dioxide

Inactive ingredients – Antiseptic Wipes aloe vera, fragrance, purified water, triethanolamine

Inactive ingredients – Triple Antibiotic Ointment petrolatum

Inactive ingredients – First Aid and Burn Cream aloe vera, emulsifying wax, ethyl alcohol, methylparaben, mineral oil, paraffin, propylparaben, purified water, white petrolatum, white wax

Inactive ingredient – Alcohol Prep Pads purified water

Inactive ingredients – Hydrocortisone Cream emulsifying wax, ethanol, methylparaben, mineral oil, paraffin, petrolatum, propylparaben, purified water, white wax

Inactive ingredients – Ibuprofen colloidal silicon dioxide, corn starch, iron oxide red, polyethylene glycol, povidone (K30), sodium starch glycolate, stearic acid, talc, titanium dioxide

🎯 Purpose 54 words

Purpose – Diphen Allergy Caplet Antihistamine

Purpose – Antiseptic Wipes Antiseptic

Purpose – Triple Antibiotic Ointment First Aid Antibiotic First Aid Antibiotic First Aid Antibiotic

Purpose – First Aid and Burn Cream First Aid Antiseptic Topical Analgesic

Purpose – Alcohol Prep Pads Antiseptic

Purpose – Hydrocortisone Cream Anti-itch

Purpose – Ibuprofen Pain reliever/fever reducer

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.