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Chest Rub Camphor, Eucalyptus Oil, Menthol 48 mg/g; 12 mg/g; 26 mg/g Cream, 50 g — NDC 41163-0248-17 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Chest Rub Camphor, Eucalyptus Oil, Menthol 48 mg/g; 12 mg/g; 26 mg/g Cream, 50 g — NDC 41163-248-17 (Billing 41163-0248-17)

by United Natural Foods, Inc. dba UNFI · 50 g in 1 JAR

This is a package of 50 g of Chest Rub Camphor, Eucalyptus Oil, Menthol 48 mg/g; 12 mg/g; 26 mg/g Cream from United Natural Foods, Inc. dba UNFI, no longer marketed (first marketed Jan 2009), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 2 package sizes.

NDC 41163-0248-17
🏷️ FDA NDC (as labeled) 41163-248-17 billing pads the product segment with a zero
This package
Contains50 g Pack sizes2 compare ↓
Main listing for product 41163-248 · Also comes in: 100 g 41163-248-75
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41163-248-17
Product NDC 41163-248
11-digit billing NDC 41163024817
UNII N20HL7Q941, 2R04ONI662, L7T10EIP3A
Application # M012
SPL Set ID b139e7d6-bf4d-45b9-b7cf-d34e5352095c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2009-01-12
Route TOPICAL
Dosage form CREAM
Substance CAMPHOR (NATURAL); EUCALYPTUS OIL; MENTHOL

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

GPI-14 90970005004000
GPI class EQL Aloe Vera After Sun
Quick answers
  • GPI-14 (Medi-Span): 90970005004000
Why two NDCs? The FDA registers this code as 41163-248-17 — 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 → 41163-0248-17. 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?

This is a topical cream containing camphor, eucalyptus oil, and menthol, marketed as an over-the-counter monograph product. These ingredients are commonly used together in chest rubs and similar products because they produce a cooling or warming sensation on the skin and are traditionally used to help open airways during breathing discomfort. The cream is applied directly to the chest or throat area.

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
41163-0248-17 You're viewing this Main listing 50 g in 1 JAR 2021-06-25 — Discontinued by firm
41163-0248-75 41163-248-75 1 JAR in 1 CARTON / 100 g in 1 JAR 2009-01-12 — Active

Pack size FAQ

What quantity is in this package?
This package contains 50 g — 50 g in 1 jar.
What NDC number is used to bill for this package of Chest Rub Camphor, Eucalyptus Oil, Menthol 48 mg/g; 12 mg/g; 26 mg/g Cream?
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 —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 41250-0824-75 Meijer, 1 jar — — Discontinued —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 21130-0248-75 Better 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/gthis 41163-0248-17 United 50 g — — Discontinued —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 63941-0248-17 Valu 1 jar — — FDA listed —
Chest Rub 48 mg/g; 12 mg/g; 26 mg/g 55319-0482-17 Family 1 jar — — 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

🏛️
2009
On the market since
Jan 2009
📍
2026
Currently FDA-listed
17 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 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 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 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.

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

The official label also statescedarleaf oil, nutmeg oil, special petrolatum, spirits of turpentine, thymol

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

LabelerUnited Natural Foods, Inc. dba UNFI
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code41163
First marketedJan 2009
Product typeHuman Otc Drug
Portfolio211 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.

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 🤒 Adverse Reactions 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 22 words ▾

Uses on chest and throat, temporarily relieves cough due to common cold on muscles and joints, temporarily releives minor aches and pains

⏱️ Dosage and Administration 70 words ▾

Directions see important warning under "When using this product" adults & children 2 yrs & over: rub a thick layer on chest & throat or rub on sore aching muscles cover with warm, dry cloth if desired keep clothing loose about throat/chest to help vapors reach the nose/mouth repeat up to three times per 24 hours or as directed by doctor children under 2 years of age: ask a doctor

⚠️ Warnings 9 words ▾

Warnings For external use only; avoid contact with eyes.

🤒 Adverse Reactions 94 words ▾

ADVERSE REACTION The active ingredients in Equaline medicated chest rub work naturally by breathing in the medicated vapors to relieve coughing due to colds. Equaline medicated chest rub also relieves minor muscle aches and pains. *This product is not manufactured or distributed by Procter & Gamble, distributor of Vicks VapoRub. Distributed by Supervalu Inc.

Eden Prairie, MN 55344 USA SUPERVALUE QUALITY GUARANTEED We're committed to your satisfaction and guarantee the quality of this product. Contact us at 1-877-932-7948, or www.supervalu-ourownbrands.com. Please have package available.

EQUALINE medicated chest rub vaporizing medicine cough suppressant topical analgesic

📦 Storage and Handling 6 words ▾

Other information store at room temperature

🧪 Active Ingredient 9 words ▾

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

🧪 Inactive Ingredients 12 words ▾

Inactive ingredients cedarleaf oil, nutmeg oil, special petrolatum, spirits of turpentine, thymol

🎯 Purpose 6 words ▾

Purpose cough suppressant & topical analgesic

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

About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 jar (41163-0248-75). 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?
United Natural Foods, Inc. dba UNFI 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.
← 41163-0241-10 · United 41163-0253-15 · United →
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.