Chest Rub Camphor, Eucalyptus Oil, Menthol 48 mg/g; 12 mg/g; 26 mg/g Jelly, 100 g — NDC 56062-248-75 (Billing 56062-0248-75)
This is a package of 100 g of Chest Rub Camphor, Eucalyptus Oil, Menthol 48 mg/g; 12 mg/g; 26 mg/g Jelly from Publix Super Markets, Inc., marketed since Apr 2021 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 56062-248-75 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 56062 labeler · 248 product · 75 package
- Package marketed since
- Apr 12, 2021
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Barcode (UPC-A, from the NDC)
- 3 5606224875 2
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 727137
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
This is a topical jelly rub containing camphor, eucalyptus oil, and menthol. These ingredients are commonly used in over-the-counter chest rubs and vapor products for their warming and cooling sensations on the skin. Camphor and menthol are topical counterirritants typically included to produce a soothing effect, while eucalyptus oil is often added for its aromatic properties. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for this category of chest rub products.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per each | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 3, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 56062-0248-75 You're viewing this Main listing | 100 g in 1 JAR | 2021-04-12 | — | Active |
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
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.
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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.
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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.
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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.
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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.
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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.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from Publix Super Markets, Inc. labeler code 56062
- maximum strength Famotidine 20 mg Tablet, Film Coated NDC 56062-194-02
- Cold Flu and Sore Throat ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE 325 mg; 10 mg; 200 mg; 5 mg Tablet, Coated NDC 56062-197-04
- Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE 325 mg; 10 mg; 200 mg; 5 mg Tablet, Coated NDC 56062-198-04
- Pseudoephedrine Hydrochloride 120 mg Tablet, Film Coated, Extended Release NDC 56062-204-21
- anti diarrheal Loperamide Hydrochloride 2 mg Tablet, Film Coated NDC 56062-224-53
- Stool Softener Laxative DOCUSATE SODIUM 100 mg Capsule, Liquid Filled NDC 56062-241-10
- dual action complete famotidine, calcium carbonate and magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable NDC 56062-263-63
- Magnesium Citrate 1.745 g/29.6mL Solution NDC 56062-264-38
- Magnesium Citrate 1.745 g/29.6mL Solution NDC 56062-266-38
- aspirin 81 mg Tablet, Chewable NDC 56062-274-68
- hemorrhoidal cocoa butter, phenylephrine HCl 2211 mg; 6.5 mg Suppository NDC 56062-279-53
- lansoprazole 15 mg Capsule, Delayed Release NDC 56062-283-01
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses on chest and throat, temporarily relieves cough due to the common cold on muscles and joints, temporarily relieves minor aches and pains
⏱️ Dosage and Administration ▾
Directions See important warnings 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 a 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 ▾
Warnings For external use only; avoid contact with eyes. Do not use by mouth with tight bandages in nostrils on wounds or damaged skin Ask a doctor before use if you have cough that occurs with too much phlegm (mucus) persistent or chronic cough such as occurs with smokng, asthma or emphysema 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 muscle aches and pains persist more than 7 days or come back cough lasts more than 7 days, comes back, or occurs with fever, rash or persistent headache. These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.
🤒 Adverse Reactions ▾
Adverse reactons DISTRIBURTED BY PUBLIX SUPER MARKETS, INC. 3300 PULBIX CORPORATE PARKWAY LAKELAND, FL 33811 publix.com PUBLIX GUARANTEE: COMPLETE SATISFACTION OR YOUR MONEY BACK
🧪 Active Ingredient ▾
Active ingredients Camphor 4.8% Eucalyptus oil 1.2% Menthol 2.6% Purpose Cough suppressant & topical analgesic
🧪 Inactive Ingredients ▾
Inactive ingredients cedarleaf oil, nutmeg oil, special petrolatum, spirits of turpentine, thymol
🎯 Purpose ▾
Purpose Cough suppressant & topical analgesic
📄 Do Not Use ▾
Do not use by mouth with tight bandages in nostrils on wounds or damaged skin
📄 Ask a Doctor Before Use If ▾
Ask a doctor before use if you have cough that occurs with too much phlegm (mucus) persistent or chronic cough such as occurs with smokng, asthma or emphysema
📄 When Using This Product ▾
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 ▾
Stop use and ask a doctor if muscle aches and pains persist more than 7 days or come back cough lasts more than 7 days, comes back, or occurs with fever, rash or persistent headache. These could be signs of a serious condition.
🤰 If Pregnant or Breast-Feeding ▾
If pregnant or breast-feeding, ask a health professional before use.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.
📄 Other Information ▾
Other information store at room temperature
📄 Package Label / Principal Display Panel ▾
principal display panel If Seal Under Cap Is Broken or Missing, DO NOT USE Only selected information is listed on the bottle label. You should keep this carton. Publix MEDICATED CHESTRUB *Compare to Vicks ® VaporRub ® COUGH SUPPRESSANT TOPICAL ANALGESIC NET WT
3.53 OZ (100 g) image description
About this NDC listing & data coverage
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. |