Chest Rub

Manufacturer
Strategic Sourcing Services LLC | Nice-Pak Products, LLC
Effective date
2026-02-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:46:13

Label at a glance#

ProductChest Rub
Active ingredientCAMPHOR (NATURAL), EUCALYPTUS OIL, MENTHOL
Label structure16 sections

Indications and uses

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

Dosage and administration

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

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

Disclaimer

SPL UNCLASSIFIED 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 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.

These 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 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

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

Adverse Reactions

ADVERSE REACTIONS SECTION

The active ingredients in Foster & Thrive Medicated Chest Rub work when you inhale in the medicated vapors to relieve coughing due to colds. Foster & Thrive Medicated Chest Rub also relieves minor muscle aches and plains. 

You may report serious side effects to 833-358-6431 Monday to Friday 9:00am to 7:00pm EST.

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

(c) 2023 McKessan Corporation

Distributed by : McKesson Corp.,

via Strategic Sourcing Servies LLC.

Memphis, TN 38141

Money Back Guarantee

www.fosterandthrive.com

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 70677-1061-1

Compare to VICKS ®VAPORUB ®*

Foster & Thrive™

Chest Rub

Menthol 2.6%

Eucalyptus Oil 1.2%

Camphor 4.8%

TOPICAL ANALGESIC

COUGH SUPPRESSANT

NET WT 3.53 OZ (100g)

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 OintmentPSN4
727137camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical OintmentSCD4
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Chest RubSY4
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical OintmentSY4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixL0021046CAmm01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70677-1061-1Chest Rub1 in 1 CARTONJELLY14
70677-1061-1Chest Rub100 g in 1 JARJELLY1004

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70677-1061-1GM - Gram70677-106181916736-bf89-4697-82f5-afa456cf8eac12023-09-05

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
70677-106170677-1061-1

Ingredients#

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

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

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, MENTHOLStrategic Sourcing Services LLCbd54bf7a-2304-4c3f-9cd2-bafea217466e2026-02-17Warnings, Adverse reactionsExact identifier
ndc (package): 70677-1061-1
ndc (product): 70677-1061
ndc11 (package): 70677106101
spl id: 4b0a4c3a-c613-dac0-e063-6294a90a15c8
spl set id: bd54bf7a-2304-4c3f-9cd2-bafea217466e

Reported adverse events (FAERS/openFDA)#

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