Vaporizing Chest Rub

Manufacturer
Universal Distribution Center LLC
Effective date
2024-10-21
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:42:09

Label at a glance#

ProductVaporizing Chest Rub
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, EUCALYPTUS OIL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Camphor            4.7%

Menthol             1.25%

Eucalyptus Oil   1.2%

OTC - PURPOSE SECTION

Purpose

Decongestant

INDICATIONS & USAGE SECTION

Uses

  • on chest and throat, helps temporarily relive cough due to common cold.
  • on joints and muscles, temporarily relives minor aches and pains.

WARNINGS SECTION

Warnings

For external use only; avoid contact with eyes.

OTC - DO NOT USE SECTION

Do not use

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

OTC - ASK DOCTOR SECTION

Ask doctor before use if you have,

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

OTC - WHEN USING SECTION

When using this product, do not

  • heat
  • microwave
  • add to hot water or any container where heating water. May cause splattering and results in burns

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • cough lasts more than 7 days, comes back, or occurs with fever, rash or persistent headache. These could be signs of a serious conditions
  • muscle aches or pain persist more than 7 days or come back

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

If ingested get medical help or contact a Poison control center immediately

DOSAGE & ADMINISTRATION SECTION

Directions

  • adults and children 2 years and over
  • rub a thick layer on chest and throat or rub on sore aching muscles
  • keep clothing loose around chest/throat to help vapors reach the nose/mouth

  • repeat up to 3 times per 24 hours or as directed by doctor
  • do not use on children under 2 years unless directed by doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients

cedar leaf oil, nutmeg oil, paraffin, petrolatum, thymol, turpentine oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

VAPORISING CHEST RUB
NASAL DECONGESTANT AND COUGH SUPPRESSANT
NET WT.4 OZ (113g)

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2045202camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical GelPSN4
2045202camphor 0.047 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.0125 MG/MG Topical GelSCD4
2045202camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-039-08Vaporizing Chest Rub50 g in 1 BOTTLE, PLASTICGEL504
52000-039-09Vaporizing Chest Rub56.6 g in 1 BOTTLE, PLASTICGEL56.64
52000-039-10Vaporizing Chest Rub100 g in 1 BOTTLE, PLASTICGEL1004
52000-039-11Vaporizing Chest Rub113 g in 1 BOTTLE, PLASTICGEL1134
52000-039-12Vaporizing Chest Rub150 g in 1 BOTTLE, PLASTICGEL1504
52000-039-13Vaporizing Chest Rub170 g in 1 BOTTLE, PLASTICGEL1704
52000-039-14Vaporizing Chest Rub226 g in 1 BOTTLE, PLASTICGEL2264

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-039VAPORIZING CHEST RUB (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]4Legacy NDC, 7 package rows20241212_cfec7539-8db6-4bdf-9a6b-3416e9afc6d9.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52000-03952000-039-08, 52000-039-09, 52000-039-10, 52000-039-11, 52000-039-12, 52000-039-13, 52000-039-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
1a836c6d-11d6-4274-8aea-c43f9c968af7cfec7539-8db6-4bdf-9a6b-3416e9afc6d92024-10-21WarningsExact identifier
spl id: 1a836c6d-11d6-4274-8aea-c43f9c968af7
spl set id: cfec7539-8db6-4bdf-9a6b-3416e9afc6d9

Reported adverse events (FAERS/openFDA)#

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