Home › NDC Lookup › Ingredients › Camphor, Eucalyptus Oil, Menthol › 00363-1001-02
Walgreens Chest Rub camphor, eucalyptus oil, menthol 48 mg/g; 12 mg/g; 26 mg/g Ointment — NDC 00363-1001-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Walgreens Chest Rub camphor, eucalyptus oil, menthol 48 mg/g; 12 mg/g; 26 mg/g Ointment — NDC 0363-1001-02 (Billing 00363-1001-02)

by Walgreen Company · 1 JAR in 1 CARTON / 50 g in 1 JAR

This is a package of Walgreens Chest Rub camphor, eucalyptus oil, menthol 48 mg/g; 12 mg/g; 26 mg/g Ointment from Walgreen Company, marketed since Mar 2015 and currently FDA-listed.

NDC 00363-1001-02
🏷️ FDA NDC (as labeled) 0363-1001-02 billing pads the labeler segment with a zero
This package
Contains50 g in 1 jar Pack sizes2 compare ↓
Product page 00363-1001-01 Also comes in: 100 g 0363-1001-01
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 0363-1001-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
0363 labeler · 1001 product · 02 package
Package marketed since
Jul 1, 2018
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 0363100102 7
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0363-1001-02
Product NDC 0363-1001
11-digit billing NDC 00363100102
NCPDP billing unit GM — per gram (weight)
RxCUI 727137
UNII 5TJD82A1ET, 2R04ONI662, L7T10EIP3A
Application # M017
SPL Set ID 3557d2e9-714a-4066-aa73-ea9e3363e574
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-03-01
Route TOPICAL
Dosage form OINTMENT
Substance CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL, UNSPECIFIED FORM

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GCN Seq No 063554
GCN 99276
HICL code 019918
Ingredient (HICL) Eucalyptus Oil/Menthol/Camphor
HIC1 code L
Therapeutic class — broad (HIC1) Skin/Subcutaneous Tissue
HIC2 code L6
Therapeutic class — intermediate (HIC2) Irritants
HIC3 code L6A
Therapeutic class — specific (HIC3) Irritants/Counter-Irritants
AHFS code 84:24.04.00
AHFS class Basic Lotions And Liniments
FDB label name CHEST RUB
FDB brand name Chest Rub
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 063554
  • GCN: 99276
  • HICL (First Databank): 019918
  • AHFS class code: 84:24.04.00
  • RxCUI (RxNorm): 727137
Why two NDCs? The FDA registers this code as 0363-1001-02 — 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 → 00363-1001-02. 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.

Clinical

Label name CHEST RUB Ingredient Eucalyptus Oil/Menthol/Camphor
🧪 What is this product?

Walgreens Chest Rub is a topical ointment containing camphor, eucalyptus oil, and menthol. These ingredients are commonly used in over-the-counter products to produce a cooling or warming sensation on the skin and are typically applied to the chest and throat area. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for this category of topical ointments rather than being individually reviewed.

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 gPer 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.
Try another pack size: 100 g
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
00363-1001-01 0363-1001-01 Main listing 1 JAR in 1 CARTON / 100 g in 1 JAR 2015-03-01 — Active
00363-1001-02 You're viewing this 1 JAR in 1 CARTON / 50 g in 1 JAR 2018-07-01 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 jar in 1 carton / 50 g in 1 jar.
What NDC number is used to bill for this package of Walgreens Chest Rub camphor, eucalyptus oil, menthol 48 mg/g; 12 mg/g; 26 mg/g Ointment?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 70677-1061-01 Strategic 1 jar $0.025 — Availability likely —
Good Neighbor Pharmacy Medicated Chest Rub .012 g/g; .048 g/g; .026 g/g 46122-0697-26 AMERISOURCE 113 g $0.026 — Availability likely —
Medicated Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 70000-0480-01 Cardinal 1 jar $0.039 — Availability likely —
Walgreens Chest Rub 48 mg/g; 12 mg/g; 26 mg/gthis 00363-1001-02 Walgreen 1 jar — — FDA listed —
Walgreens Chest Rub 26 mg/g; 48 mg/g; 12 mg/g 00363-1004-01 Walgreen 1 jar — — FDA listed —
Walgreens Childrens Chest Rub 26 mg/g; 48 mg/g; 12 mg/g 00363-9800-01 Walgreen 1 jar — — FDA listed —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 11344-0248-17 Nice-Pak 1.76 g — — FDA listed —
Medicated Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 11673-0501-59 TARGET 49.8 g — — FDA listed —
cough suppressant and topical analgesic 48 mg/g; 12 mg/g; 26 mg/g 11673-0667-02 Target 1 jar — — FDA listed —
Rite Aid Chest Rub .048 g/g; .012 g/g; .026 g/g 11822-4205-01 Rite 1 jar — — FDA listed —
Rite Aid Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 11822-8545-02 Rite 1 jar — — FDA listed —
Vapor Rub .026 g/g; .048 g/g; .012 g/g 13709-0336-01 Neilmed 1 jar — — FDA listed —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 21130-0248-75 Better 1 jar — — FDA listed —
Vaporex 4.8 g/100g; 1.2 g/100g; 2.6 g/100g 24286-1564-03 DLC 1 jar — — FDA listed —
Bactimicina Vapor Rub 4.8 g/100g; 1.2 g/100g; 2.6 g/100g 24286-1580-02 DLC 1 jar — — FDA listed —
Earths Care Chest Rub 4.8 g/100g; 2.6 g/100g; 1.2 g/100g 24286-1581-02 DLC 1 jar — — FDA listed —
Chest Rub 26 mg/g; 48 mg/g; 12 mg/g 27854-0399-00 Belmora 1 jar — — FDA listed —
24/7 Life Medicated Chest Rub 1.2 g/100g; 4.8 g/100g; 2.6 g/100g 29485-6536-04 Lil' 1 jar — — FDA listed —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 30142-0248-17 The 1 jar — — FDA listed —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 36800-0596-75 Topco 1 jar — — FDA listed —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 37808-0248-75 H 100 g — — FDA listed —
Chest Rub 26 mg/g; 48 mg/g; 12 mg/g 42507-0248-75 Hy-Vee, 1 jar — — FDA listed —
Equate Childrens Vaporizing 48 mg/g; 12 mg/g; 26 mg/g 49035-0770-01 Wal-Mart 1 jar — — FDA listed —
Equate Vaporizing 48 mg/g; 12 mg/g; 26 mg/g 49035-0872-72 Wal-Mart 1 jar — — FDA listed —
GoodSense Medicated Chest Rub .048 g/g; .012 g/g; .026 g/g 50804-0205-01 GOOD 1 jar — — FDA listed —
Chest Rub 4.8 g/100g; 1.2 g/100g; 2.6 g/100g 51628-4242-01 MY 113 g — — FDA listed —
CareAll Medicated Chest Rub .048 g/g; .026 g/g; .012 g/g 51824-0045-03 New 100 g — — Discontinued —
Viva Porru Chest Rub .012 g/g; .048 g/g; .026 g/g 53145-0707-02 Menper 57 g — — FDA listed —
Chest Rub 12 mg/g; 26 mg/g; 48 mg/g 55301-0248-75 Your 1 jar — — FDA listed —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 55319-0482-17 Family 1 jar — — FDA listed —
Medicated Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 55910-0833-05 DOLGENCORP, 100 g — — FDA listed —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 56062-0248-75 Publix 100 g — — FDA listed —
Vaporizing Chest Rub 4 oz. 4.8 g/100mL; 1.2 g/100mL; 2.6 g/100mL 57337-0097-01 Rejoice 1 jar — — FDA listed —
Vaporizing Chest Rub 4 oz. 3 pk 4.8 g/100mL; 1.2 g/100mL; 2.6 g/100mL 57337-0099-01 Rejoice 3 jars — — FDA listed —
Vicks VapoRub .048 g/g; .012 g/g; .026 g/g 58933-0544-01 Procter 1 jar — — FDA listed —
Vicks childrens VapoRub .048 g/g; .012 g/g; .026 g/g 58933-0595-50 Procter 1 jar — — FDA listed —
CVS Health Medicated Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 59779-0790-01 CVS 1 jar — — FDA listed —
Quality Choice Medicated Chest Rub .012 g/g; .048 g/g; .026 g/g 63868-0800-04 QUALITY 113 g — — FDA listed —
Vicks VapoRub ADVANCED PLUS .012 g/g; .026 g/g; .048 g/g 64336-0001-01 Procter 1 jar — — FDA listed —
Winco Foods Medicated Chest Rub .048 g/g; .012 g/g; .026 g/g 67091-0410-04 WinCo 1 jar — — FDA listed —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 68016-0248-75 Pharmacy 1 jar — — FDA listed —
HealthWise Chest Rub Lavender .012 g/g; .048 g/g; .026 g/g 71101-0027-01 Veridian 100 g — — FDA listed —
HealthWise Chest Rub Lemon .012 g/g; .048 g/g; .026 g/g 71101-0028-01 Veridian 100 g — — FDA listed —
HealthWise Medicated Chest Rub .048 g/g; .012 g/g; .026 g/g 71101-0036-01 Veridian 1 jar — — FDA listed —
TheraCare Medicated Chest Rub .048 g/g; .012 g/g; .026 g/g 71101-0200-01 Veridian 1 jar — — FDA listed —
TheraCare Medicated Chest Rub .012 g/g; .048 g/g; .026 g/g 71101-0202-01 Veridian 100 g — — FDA listed —
HealthWise Chest Rub .048 g/g; .012 g/g; .026 g/g 71101-0205-01 Veridian 1 jar — — FDA listed —
Vaporx .048 g/g; .012 g/g; .026 g/g 71399-4589-01 AKRON 100 g — — FDA listed —
Vaporizing Rub 2.4 g/50g; 1.3 g/50g; .6 g/50g 73492-0716-50 ALAINA 1 jar — — FDA listed —
SofSkin Vaporizing Chest Rub and Cough Suppressant 4.8 g/100g; 2.6 g/100g; 1.2 g/100g 76436-0144-14 Viny 113 g — — FDA listed —
Meijer Medicated Chest Rub, 3.53 oz. Lavender 4.8 g/100g; 1.2 g/100g; 2.6 g/100g 79481-9928-01 Meijer 50 g — — FDA listed —
Equate Rub 2.6 g/100g; 4.8 g/100g; 1.2 g/100g 79903-0194-17 Walmart 1 jar — — FDA listed —
Caring Mill Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 81522-0725-01 FSA 1 jar — — FDA listed —
Quality Choice Medicated Chest Rub .012 g/g; .048 g/g; .026 g/g 83324-0261-04 Quality 113 g — — 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

🏛️
2015
On the market since
Mar 2015
📍
2026
Currently FDA-listed
11 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 3J50XA376E
    Thymol is a natural compound derived from thyme and other plants. It acts as a preservative and flavoring agent in medicines, helping prevent microbial growth and add taste.
  • UNII C5H0QJ6V7F
    Turpentine oil is a volatile liquid extracted from pine tree resin. It's used in some formulations as a solvent and flavoring agent to help dissolve other ingredients and add taste.

3 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesfragrance, petrolatum, thymol, turpentine oil

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.

Manufacturer & labeler

LabelerWalgreen Company
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code00363
First marketedMar 2015
Product typeHuman Otc Drug
Portfolio468 products on file

More NDCs from Walgreen Company 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Ask a Doctor 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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 25 words ▾

Uses temporarily relieves cough due to minor throat and bronchial irritation associated with a cold temporarily relieves minor aches and pains of muscles and joints

⏱️ Dosage and Administration 80 words ▾

Directions see important warning under "When using this product" adults and children 2 years and over: rub a thick layer on the throat and chest for cough, or rub on sore aching muscles and joints cover with a warm, dry cloth if desired clothing should be left loose about the throat and chest to help vapors reach the nose and mouth use up to 3 times daily, or as directed by a doctor children under 2 years: ask a doctor

⚠️ Warnings 147 words ▾

Warnings For external use only Ask a doctor before use if you have cough that occurs with too much phlegm (mucus) chronic cough that lasts or occurs with smoking, asthma, or emphysema When using this product do not heat, microwave, or add to hot water or any container where heating water. May cause splattering and result in burns. do not take by mouth or place in nostrils do not get into eyes do not apply to wounds or damaged skin do not bandage tightly Stop use and ask a doctor if 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. muscle aches and pains worsen, persist for more than 7 days, or clear up and occur again within a few days If pregnant or breast-feeding ask a health professional before use

🧪 Active Ingredient 9 words ▾

Active ingredient Camphor 4.8% Eucalyptus oil 1.2% Menthol 2.6%

🧪 Inactive Ingredients 7 words ▾

Inactive Ingredients fragrance, petrolatum, thymol, turpentine oil

🎯 Purpose 16 words ▾

Purpose Camphor – Cough suppressant/topical analgesic Eucalyptus oil – Cough suppressant Menthol – Cough suppressant/topical analgesic

📄 Ask a Doctor Before Use If 27 words ▾

Ask a doctor before use if you have cough that occurs with too much phlegm (mucus) chronic cough that lasts or occurs with smoking, asthma, or emphysema

📄 When Using This Product 52 words ▾

When using this product do not heat, microwave, or add to hot water or any container where heating water. May cause splattering and result in burns. do not take by mouth or place in nostrils do not get into eyes do not apply to wounds or damaged skin do not bandage tightly

📄 Stop Use and Ask a Doctor If 53 words ▾

Stop use and ask a doctor if 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. muscle aches and pains worsen, persist for more than 7 days, or clear up and occur again within a few days

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding ask a health professional before use

📄 Keep Out of Reach of Children 21 words ▾

Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

📄 Package Label / Principal Display Panel 5 words ▾

Package/Label Principal Display Panel Carton

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 Camphor, eucalyptus oil, menthol — the ingredient across all brands.

Top reported reactions

Fatigue15
Dyspnoea14
Dizziness12
Headache12
Anxiety11
Chronic Kidney Disease11
Pain11

Age at onset

Child2
Adult14
Elderly21

Reporter sex

234 reports
Male · 32%
Female · 68%

Serious outcomes

Hospitalization46
Disabling10
Life-threatening7
Death6
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 12 0
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.

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

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 Company. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 jar (00363-1001-01). Each has its own NDC and its own page — see the package list near the top of this page.
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.
← 00363-0997-48 · WALGREEN 00363-1002-40 · 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.