Home › NDC Lookup › Ingredients › Camphor, Eucalyptus Oil, Menthol › 64336-0001-02
Vicks VapoRub ADVANCED PLUS Camphor, Eucalyptus oil, Menthol .012 g/g; .026 g/g; .048 g/g Ointment — NDC 64336-0001-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Vicks VapoRub ADVANCED PLUS Camphor, Eucalyptus oil, Menthol .012 g/g; .026 g/g; .048 g/g Ointment — NDC 64336-001-02 (Billing 64336-0001-02)

by Procter & Gamble Manufacturing GmbH · 1 JAR in 1 CARTON / 80 g in 1 JAR

This is a package of Vicks VapoRub ADVANCED PLUS Camphor, Eucalyptus oil, Menthol .012 g/g; .026 g/g; .048 g/g Ointment from Procter & Gamble Manufacturing GmbH, marketed since Jul 2023 and currently FDA-listed.

NDC 64336-0001-02
🏷️ FDA NDC (as labeled) 64336-001-02 billing pads the product segment with a zero
This package
Contains80 g in 1 jar Pack sizes3 compare ↓
Product page 64336-0001-01 Also comes in: 50 g 64336-001-01 2 jars 64336-001-03
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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 64336-001-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
64336 labeler · 001 product · 02 package
Package marketed since
Jul 6, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 6433600102 6
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 64336-001-02
Product NDC 64336-001
11-digit billing NDC 64336000102
Application # M012
SPL Set ID f801128c-94bb-fa9e-e053-6294a90a0822
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-07-06
Route TOPICAL
Dosage form OINTMENT
Substance EUCALYPTUS OIL; MENTHOL, UNSPECIFIED FORM; CAMPHOR (SYNTHETIC)
Why two NDCs? The FDA registers this code as 64336-001-02 — 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 → 64336-0001-02. 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

🧪 What is this product?

Vicks VapoRub Advanced Plus is a topical ointment containing camphor, eucalyptus oil, and menthol. These ingredients are commonly used in over-the-counter rub products and are typically applied to the skin for temporary relief of minor aches and to help open airways. Camphor, eucalyptus oil, and menthol produce a cooling or warming sensation on the skin and are often included in vapor rubs intended to ease discomfort from colds or congestion. This product is marketed as an over-the-counter monograph drug, meaning it follows established FDA guidelines for this category rather than undergoing individual product approval.

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: 50 g 2 jars
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
64336-0001-01 64336-001-01 Main listing 1 JAR in 1 CARTON / 50 g in 1 JAR 2023-07-06 — Active
64336-0001-02 You're viewing this 1 JAR in 1 CARTON / 80 g in 1 JAR 2023-07-06 — Active
64336-0001-03 64336-001-03 2 JAR in 1 CELLO PACK / 80 g in 1 JAR 2023-07-06 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 jar in 1 carton / 80 g in 1 jar.
What NDC number is used to bill for this package of Vicks VapoRub ADVANCED PLUS Camphor, Eucalyptus oil, Menthol .012 g/g; .026 g/g; .048 g/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/g 00363-1001-01 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/gthis 64336-0001-02 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

🏛️
2023
On the market since
Jul 2023
📍
2026
Currently FDA-listed
3 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.

What it looks like

Color white
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 BJ169U4NLG
    Cedar leaf oil is a fragrant extract from cedar tree foliage used as a flavoring agent and fragrance in medications to improve taste and aroma, making the medicine more pleasant to take.
  • UNII Q6CA504696
    A synthetic organic compound used as a flavoring agent and sensory enhancer in medicines. It provides a cooling or minty sensation and improves the taste profile of oral formulations.
  • UNII Z1CLM48948
    Nutmeg oil is a natural aromatic extract from nutmeg seeds. It's used in medicines as a flavoring agent to improve taste and sometimes as a fragrance to mask bitter or unpleasant odors.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • 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.

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

The official label also statescedarleaf oil, nutmeg oil, paraffin, petrolatum, Symcool ® WS-5 (menthane carboxamidoethyl acetate), 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

LabelerProcter & Gamble Manufacturing GmbH
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code64336
First marketedJul 2023
Product typeHuman Otc Drug
Portfolio7 products on file

More NDCs from Procter & Gamble Manufacturing GmbH labeler code 64336

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 🆘 Overdosage 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 40 words ▾

Uses • when applied to chest and throat, temporarily relieves cough due to minor throat and bronchial irritation associated with the common cold • when applied to muscles and joints, temporarily relieves minor aches and pains of muscles and joints

⏱️ Dosage and Administration 97 words ▾

Directions • see important warnings under “When using this product” • adults and children 2 years and over: • for cough suppression • rub a thick layer on throat & chest • cover with a warm, dry cloth if desired • keep clothing loose about throat and chest to help vapors reach the nose and mouth • use up to three times daily or as directed by doctor • for muscle / joint minor aches and pains apply to affected area not more than 3 to 4 times daily • children under 2 years: do not use

⚠️ Warnings 9 words ▾

Warnings For external use only; avoid contact with eyes.

🆘 Overdosage 13 words ▾

If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 10 words ▾

Other information • store at no greater than 25°C (77°F)

🧪 Active Ingredient 10 words ▾

Active ingredients Camphor (synthetic) 4.8% Eucalyptus oil 1.2% Menthol 2.6%

🧪 Inactive Ingredients 17 words ▾

Inactive ingredients cedarleaf oil, nutmeg oil, paraffin, petrolatum, Symcool ® WS-5 (menthane carboxamidoethyl acetate), thymol, turpentine oil

🎯 Purpose 15 words ▾

Active ingredients Purpose Cough suppressant & topical analgesic Cough suppressant Cough suppressant & topical analgesic

📄 Do Not Use 19 words ▾

Do not use • by mouth • in nostrils • on wounds or damaged skin • with tight bandages

📄 Ask a Doctor Before Use If 30 words ▾

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

📄 When Using This Product 28 words ▾

When using this product do not • heat • microwave • add to hot water or any container where heating water. May cause splattering and result in burns.

📄 Stop Use and Ask a Doctor If 61 words ▾

Stop use and ask a doctor if • muscle aches and pains worsen or persist for more than 7 days or clear up and occur again within a few days. • cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.

🤰 If Pregnant or Breast-Feeding 10 words ▾

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

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Questions or Comments 2 words ▾

Questions? 1-800-873-8276

📄 Package Label / Principal Display Panel 36 words ▾

PRINCIPAL DISPLAY PANEL -

2.82OZ (80 g) jar NEW VICKS ® VapoRub™ ADVANCED PLUS COUGH SUPPRESSANT TOPICAL ANALGESIC POWERFUL COUGH RELIEF VAPORS LAST UP TO 8 HOURS NET WT

2.82 OZ (80 g) OINTMENT 001

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

Serious outcomes

Hospitalization46
Life-threatening7
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 9 1
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 Procter & Gamble Manufacturing GmbH. 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 2 other package presentations of this same product, including 1 jar (64336-0001-01), 2 jars (64336-0001-03). 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?
Procter & Gamble Manufacturing GmbH 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.
← 64330-0670-01 · Centaur 64336-0002-01 · Procter →
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.