FDA.reportPublic FDA data

Chest Rub

Manufacturer
Topco Associates LLC | Nice-Pak Products, LLC
Effective date
2026-02-13
Label type
HUMAN OTC DRUG LABEL
Version
15
Source
full-release
Hydrated at
2026-06-01 01:44:17

Label at a glance#

ProductChest Rub
Active ingredientCAMPHOR (SYNTHETIC), EUCALYPTUS OIL, MENTHOL
Label structure10 sections

Indications and 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

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

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

Additional warnings

WARNINGS AND PRECAUTIONS SECTION

Failure to follow these warnings could result in serious consequences  

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 4.8%

Eucalyptus oil 1.2%

Menthol 2.6%

Purpose

OTC - PURPOSE SECTION

Cough suppressant & topical analgesic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only; avoid contact with eyes.

Do not use

OTC - DO NOT USE SECTION

  • by mouth
  • with tight bandages
  • in nostrils
  • on wounds or damaged skin

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • cough that occurs with too much phlegm (mucus)
  • persistent or chronic cough such as occurs with smoking, asthma or emphysema

When using this product, do not

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

  • 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.

This could be signs of a serious condition.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

  • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

Call 1-888-423-0139

ADVERSE REACTION

ADVERSE REACTIONS SECTION

The active ingredients in Top Care Vaporizing Rub work when you inhale in the medicated vapors to relieve coughing due to colds. Top Care Vaporizing Rub also relieves monor muscle aches and pains.

*This product is not manufactured or distributed by Procter & Gamble, distributor of Vicks ®VapoRub ®

DISTRIBUTED BY: TOPCO ASSOCIATES LLC

ELK GROVE VILLAGE, IL 60077

TOPCO  VIJA0521

QUESTIONS? 1-888-423-0139

topcare@topco.com   www.topcarebrand.com

Scan here for more information or call 1-888-423-0139

Qualiy Guaranteed

This TopCare ®product is laboratory tested to guarantee its highest quality. Your totla satisfaction is guaranteed.

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TopCare ®

health

COMPARE TO VICKS ®VAPORUB ®ACTIVE INGREDIENTS*

Vaporizing

Rub

COUGH SUPPRESSANT

TOPICAL ANALGESIC

  • Relives Coughing Due to Colds
  • Relieves Minor Muscle Aches and Pains
  • Soothing Ointment

NET WT 3.53 OZ (100 g)

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical OintmentPSN15
727137camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical OintmentSCD15
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Chest RubSY15
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical OintmentSY15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36800-596-75Chest Rub100 g in 1 JARJELLY10015
36800-596-75Chest Rub1 in 1 CARTONJELLY115

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
36800-59636800-596-75

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
NUTMEG OILZ1CLM48948IACT
CEDAR LEAF OILBJ169U4NLGIACT
PETROLATUM4T6H12BN9UIACT
TURPENTINE OILC5H0QJ6V7FIACT
THYMOL3J50XA376EIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
EUCALYPTUS OIL2R04ONI662ACTIB
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Chest RubCAMPHOR, EUCALYPTUS OIL, MENTHOLTopco Associates LLC62eed0e8-ba5f-45c2-a543-68b50bcf4b0c2026-02-13Warnings, Adverse reactionsExact identifier
ndc (package): 36800-596-75
ndc (product): 36800-596
ndc11 (package): 36800059675
spl id: 4ab830b3-a6d9-de01-e063-6394a90a41b3
spl set id: 62eed0e8-ba5f-45c2-a543-68b50bcf4b0c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.