Vaporizing Cold Rub

Manufacturer
Delon Laboratories (1990) Ltd | Laboratoires Delon
Effective date
2026-06-18
Label type
HUMAN OTC DRUG LABEL
Version
28
Source
monthly-update
Hydrated at
2026-07-17 21:34:29

Label at a glance#

ProductVaporizing Colds Rub
Active ingredientMENTHOL, EUCALYPTUS OIL, CAMPHOR (SYNTHETIC)
Label structure12 sections

Indications and uses

temporarily relieves: cough due to minor bronchial irritation associated with a cold or inhaled irritants cough associated with a cold minor aches and pains of muscles and joints

Dosage and administration

see important warnings under "When using this product" adults and children 2 years and older: rub on the throat and chest in a thick layer cover with a warm, dry cloth if desired clothing should be loose about throat and chest to help vapors reach the nose and mouth use up to three times daily or as directed by a doctor children under 2 years of age: ask a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 4.7%
Eucalyptus oil 1.2%
Menthol 2.6%


Purpose

OTC - PURPOSE SECTION

Cough suppressant & topical analgesic

Cough suppressant

Cough suppressant & topical analgesic

Uses

INDICATIONS & USAGE SECTION

temporarily relieves:

  • cough due to minor bronchial irritation associated with a cold or inhaled irritants
  • cough associated with a cold
  • minor aches and pains of muscles and joints

Warnings

WARNINGS SECTION

For external use only; avoid contact with eyes.

Do not use:

OTC - DO NOT USE SECTION

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • excessive phlegm (mucus)
  • emphysema
  • persistent or chronic cough
  • asthma
  • cough associated with smoking

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 worsen or persist for more than 7 days or clear up and occur again within a few days
  • cough perists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • see important warnings under "When using this product"
  • adults and children 2 years and older:
  • rub on the throat and chest in a thick layer
  • cover with a warm, dry cloth if desired
  • clothing should be loose about throat and chest to help vapors reach the nose and mouth
  • use up to three times daily or as directed by a doctor
  • children under 2 years of age: ask a doctor

Other information

OTHER SAFETY INFORMATION

  • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

cedar leaf oil, petrolatum, thymol, turpentine

Penetro1.75oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Penetro Vaporizing Rub 1.75oz BoxPenetro Vaporizing Rub 1.75oz Box

Penetro 1.75 oz Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Penetro VCR 1.75 oz LabelPenetro VCR 1.75 oz Label

Penetro4oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Penetro Vaporizing Medicated Rub 4oz boxPenetro Vaporizing Medicated Rub 4oz box

Penetro 4oz Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Penetro VCR 4oz LabelPenetro VCR 4oz Label

PII 4 OZ

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PII Vaporizing Colds Rub 4 ozPII Vaporizing Colds Rub 4 oz

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Camphor (Synthetic)ACTIVE INGREDIENT5TJD82A1ET7
Eucalyptus OilACTIVE INGREDIENT2R04ONI6627
MentholACTIVE INGREDIENTL7T10EIP3A7
Camphor (Synthetic)ACTIVE MOIETY5TJD82A1ET7
Eucalyptus OilACTIVE MOIETY2R04ONI6627
MentholACTIVE MOIETYL7T10EIP3A7
Cedar Leaf OilINACTIVE INGREDIENTBJ169U4NLG7
Mineral OilINACTIVE INGREDIENTT5L8T28FGP7
PetrolatumINACTIVE INGREDIENT4T6H12BN9U7
ThymolINACTIVE INGREDIENT3J50XA376E7
TurpentineINACTIVE INGREDIENTXJ6RUH0O4G7

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61734-03061734-030-04, 61734-030-02, 61734-030-03, 61734-030-05

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
272025-10-16full-release2026-06-01 01:39:18
262025-02-07full-release2026-06-01 00:54:48

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 20 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
PetrolatumPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
Mineral OilMINERAL OILT5L8T28FGPOINTMENT / TOPICAL9938 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
PetrolatumPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
ThymolTHYMOL3J50XA376ELIQUID / RESPIRATORY (INHALATION)0.01 %w/wExact identifier — unii candidate
10 equally ranked IID candidates
PetrolatumPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
ThymolTHYMOL3J50XA376EPOWDER, FOR SOLUTION / ORALNAExact identifier — unii candidate
10 equally ranked IID candidates
PetrolatumPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
ThymolTHYMOL3J50XA376EPOWDER, FOR SOLUTION / ORALNAExact identifier — unii candidate
10 equally ranked IID candidates
ThymolTHYMOL3J50XA376ELIQUID / RESPIRATORY (INHALATION)0.01 %w/wExact identifier — unii candidate
10 equally ranked IID candidates
ThymolTHYMOL3J50XA376ELIQUID / RESPIRATORY (INHALATION)0.01 %w/wExact identifier — unii candidate
10 equally ranked IID candidates
ThymolTHYMOL3J50XA376EPOWDER, FOR SOLUTION / ORALNAExact identifier — unii candidate
10 equally ranked IID candidates
ThymolTHYMOL3J50XA376ELIQUID / RESPIRATORY (INHALATION)0.01 %w/wExact identifier — unii candidate
10 equally ranked IID candidates
PetrolatumPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
ThymolTHYMOL3J50XA376ELIQUID / RESPIRATORY (INHALATION)0.01 %w/wExact identifier — unii candidate
10 equally ranked IID candidates
Mineral OilMINERAL OILT5L8T28FGPOINTMENT / TOPICAL9938 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
ThymolTHYMOL3J50XA376EPOWDER, FOR SOLUTION / ORALNAExact identifier — unii candidate
10 equally ranked IID candidates
Mineral OilMINERAL OILT5L8T28FGPOINTMENT / TOPICAL9938 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
Mineral OilMINERAL OILT5L8T28FGPOINTMENT / TOPICAL9938 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
Mineral OilMINERAL OILT5L8T28FGPOINTMENT / TOPICAL9938 mgExact identifier — unii+route+dosage form
5 equally ranked IID candidates
ThymolTHYMOL3J50XA376EPOWDER, FOR SOLUTION / ORALNAExact identifier — unii candidate
10 equally ranked IID candidates

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
Vaporizing Colds RubMENTHOLDelon Laboratories (1990) Ltd3ed8bc0c-c229-450b-a491-06b578c1b8ee2026-06-18WarningsExact identifier
ndc (package): 61734-030-04
ndc (package): 61734-030-05
ndc (package): 61734-030-03
ndc (package): 61734-030-02
ndc (product): 61734-030
ndc11 (package): 61734003005
ndc11 (package): 61734003004
ndc11 (package): 61734003002
ndc11 (package): 61734003003
spl id: 5488afee-9d3b-ff80-e063-6394a90a29f9
spl set id: 3ed8bc0c-c229-450b-a491-06b578c1b8ee

Reported adverse events (FAERS/openFDA)#

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