FDA.reportPublic FDA data

MEDICATED CHEST RUB

Manufacturer
GOODSENSE | Natureplex LLC
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:50:17

Label at a glance#

ProductMEDICATED CHEST RUB
Active ingredientCAMPHOR (SYNTHETIC), EUCALYPTUS OIL, MENTHOL, UNSPECIFIED FORM
Label structure10 sections

Indications and uses

on chest & 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 and children 2 years old and older: rub a thick layer on chest & throat for cough, or rub on sore aching muscles or joints 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 daily or as directed by a doctor Children under 2 years: do not use

Storage and handling

store at 15 to 30°C (59 to 86°F) Tamper Evident: DO NOT USE IF SEAL ON JAR IS BROKEN OR MISSING.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientsPurposes
Camphor 4.8%Cough suppressant & topical analgesic
Eucalyptus oil 1.2%Cough suppressant
Menthol 2.6%Cough suppressant & topical analgesic

Uses

INDICATIONS & USAGE SECTION

  • on chest & 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

OTC - WHEN USING SECTION

  • do not heat
  • do not microwave
  • do not 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 worsen, persist for more than 7 days, or clear up and occur again within a few days
  • cough lasts more than 7 days, tends to recur, or occurs with fever, rash, or persistent headache. These could be signs of a serious condition.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

see important warnings under "When using this product"

  • Adults and children 2 years old and older:
    • rub a thick layer on chest & throat for cough, or rub on sore aching muscles or joints
    • 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 daily or as directed by a doctor
  • Children under 2 years: do not use

Other information

STORAGE AND HANDLING SECTION

  • store at 15 to 30°C (59 to 86°F)
  • Tamper Evident: DO NOT USE IF SEAL ON JAR IS BROKEN OR MISSING.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions or comments?

OTC - QUESTIONS SECTION

866-323-0107

SPL UNCLASSIFIED SECTION

Distributed by: Geiss, Destin & Dunn, Inc.
Peachtree City, GA 30269

PRINCIPAL DISPLAY PANEL - 100 g Jar Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GOODSENSE®
NDC# 50804-078-01

Medicated
Chest Rub

  • Nasal Decongestant
  • Cough Suppressant
  • Topical Analgesic

Compare to active ingredients of
Vicks® VapoRub®*

100%
SATISFACTION
GUARANTEED

NET WT 3.53 OZ (100 g)

Principal Display Panel - 100 g Jar Label
Principal Display Panel - 100 g Jar Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical OintmentPSN2
727137camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical OintmentSCD2
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Chest RubSY2
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical OintmentSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50804-078-01MEDICATED CHEST RUB100 g in 1 JAROINTMENT1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50804-078MEDICATED CHEST RUB (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL, UNSPECIFIED FORM) OINTMENT [GOODSENSE]2Legacy NDC, 1 package rows20250101_f18ff94f-8716-4514-93f8-e101867e1c8b.zip

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
50804-07850804-078-01

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
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
EUCALYPTUS OIL2R04ONI662ACTIB
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
CEDAR LEAF OILBJ169U4NLGIACT
NUTMEG OILZ1CLM48948IACT
TURPENTINE OILC5H0QJ6V7FIACT
THYMOL3J50XA376EIACT
WHITE PETROLATUMB6E5W8RQJ4IACT

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
f9bef353-54e5-4ad4-8170-7126e5c388bff18ff94f-8716-4514-93f8-e101867e1c8b2024-12-31WarningsExact identifier
spl id: f9bef353-54e5-4ad4-8170-7126e5c388bf
spl set id: f18ff94f-8716-4514-93f8-e101867e1c8b

Reported adverse events (FAERS/openFDA)#

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