Vicks Vaporub

Manufacturer
Genesis Imports & Exports | Teresa Cecena | Genesis Imports & Exports LLC | procter & Gamble Manufactura S De RL De CV | Roir SA de CV
Effective date
2017-12-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:53:45

Label at a glance#

ProductVicks Vaporub
Active ingredientEUCALYPTUS OIL, CAMPHOR (SYNTHETIC), MENTHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Camphor 4.8 %

Eucalyptus oil 1.2%

Menthol 2.63%

OTC - PURPOSE SECTION

Cough suppressant & topical analgesic,

Cough suppressant

DOSAGE & ADMINISTRATION SECTION

* On Chest and throat, temporarily relieves cough due to common cold

* On Muscles and joins, temporarily relieves minor aches and pains

WARNINGS SECTION

Warnings

For external use only; avoid contact with eyes.

Do Not Use

* By mouth

*With tight bandages

*In nostrils

*On wounds or damaged skin

OTC - ASK DOCTOR SECTION

Ask A doctor use if you have:

*cough that occurs with too much phlegm (mucus)

*Persistent or chronic such as occurs with smoking, asthma or emplysema

OTC - WHEN USING SECTION

When use this product, do not

* HEat

* Microware

* Add to hot water or any container where heating water.

May cause splattering and result in burns

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

INDICATIONS & USAGE SECTION

Directions:

See important warnings under when using this product

  • adults and children 2 years and over:
  1. RUB A THICK LAYER ON CHEST & THROAT OR RUB ON SORE ACHING MISCLES
  2. Cover with a warm, dry cloth if desired
  3. Keep clothing loose abouth throat/chest to help vapors reach the nose/ mouse
  4. repeat up three times per 24 hours or as directed by doctor
  5. children under 2 yearsL do not use.

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Cedarleaf oil, nutmeg oil, special petrolatum, thymol, turpentine oil.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Net Wt 3.52 Oz 100GrNet Wt 3.52 Oz 100Gr

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69772-390-01Vicks Vaporub100 g in 1 JAROINTMENT1002
69772-390-02Vicks Vaporub50 g in 1 JAROINTMENT502
69772-390-03Vicks Vaporub12 g in 1 JAROINTMENT122

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69772-390VICKS VAPORUB (CAMPHOR, EUCALYPTUS OIL, AND MENTHOL OILMENT) OINTMENT [GENESIS IMPORTS & EXPORTS]2Legacy NDC, 3 package rows20171228_420fb0e7-73a4-0500-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69772-39069772-390-01, 69772-390-02, 69772-390-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML · Source PDF

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
616b0caa-c2b8-0024-e053-2991aa0a51a9420fb0e7-73a4-0500-e054-00144ff8d46c2017-12-28WarningsExact identifier
spl id: 616b0caa-c2b8-0024-e053-2991aa0a51a9
spl set id: 420fb0e7-73a4-0500-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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