FDA.reportPublic FDA data

Pharmacys Prescription Vapor Rub

Manufacturer
American Consumer Products Corp
Effective date
2021-02-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:02

Label at a glance#

ProductPharmacys Prescription Vapor Rub
Active ingredientMENTHOL, UNSPECIFIED FORM, EUCALYPTUS OIL, CAMPHOR (SYNTHETIC)
Label structure10 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Camphor 4.7%

Menthol 1.25%

Eucalyptus Oil 1.2%

Purpose

OTC - PURPOSE SECTION

Purpose

Decongestant

Decongestant

Decongestant

Indications & Usage

INDICATIONS & USAGE SECTION

USE:

To temporarily relieve nasal congestion, chest congestion and cough due to the common cold. Temporarily relieves minor aches and pains.

Warning

WARNINGS SECTION

Warning: For external use only. Not for internal use. Avoid contact with eyes. Do not put in mouth, nostrils, or on wounds or damaged skin.

If Pregnant or Breast Feeding

NURSING MOTHERS SECTION

If pregnant or breast feeding, consult a physician before use. Do not use near open flame, in a microwave oven or in a container in which water is being heated except when adding to cold water in a hot steam vaporizer.

Consult a Physician Before Use

OTC - ASK DOCTOR SECTION

Consult a physician before use. If you have asthma, emphysema, persistent or chronic cough associated with smoking or excessive mucus. If muscle aches persist for more than 7 days or comes back, or cough lasts more than 7 days, comes back or occurs with fever, rash or a persistent headache.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If ingested, get medical help or contact a Poison Control Center right away.

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Directions:Adults and children 2 years of age and older, rub a thick layer on chest and throat for temporary relief from nasal congestion and coughing due to colds, or rub on sore aching aching muscles. If desired, loosely cover with a soft dry cloth, but keep clothing loose. Repeat up to three times daily, especially at bedtime. Children under 2 years of age, consult your physician.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Petrolatum, Thymol, Turpentine, Cedar Wood Oil, Nutmeg Oil.

Pharmacy's Prescription 4 OZ Vapor Rub

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vapor RubVapor Rub

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2045202camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical GelPSN1
2045202camphor 0.047 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.0125 MG/MG Topical GelSCD1
2045202camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-042-042023-01-30C16284748780-1f386c64a-2d3a-0266-e053-dadaa90a7c1aPharmacy's Prescription 4 OZ Vapor Rub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-042-04Pharmacys Prescription Vapor Rub110 g in 1 BOTTLE, PLASTICGEL1101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-042PHARMACYS PRESCRIPTION VAPOR RUB (MENTHOL) GEL [AMERICAN CONSUMER PRODUCTS CORP]1Legacy NDC, 1 package rows20210211_baec2b90-6895-4476-e053-2995a90a81ec.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
72197-04272197-042-04

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
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
EUCALYPTUS OIL2R04ONI662ACTIB
PETROLATUM4T6H12BN9UIACT
NUTMEG OILZ1CLM48948IACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
CEDAR LEAF OILBJ169U4NLGIACT
TURPENTINE OILC5H0QJ6V7FIACT
THYMOL3J50XA376EIACT

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
baec49db-ac9b-0226-e053-2995a90a84d9baec2b90-6895-4476-e053-2995a90a81ec2021-02-09WarningsExact identifier
spl id: baec49db-ac9b-0226-e053-2995a90a84d9
spl set id: baec2b90-6895-4476-e053-2995a90a81ec

Reported adverse events (FAERS/openFDA)#

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