Vaporizing Chest Rub

Manufacturer: Quality Care Distributors LLC | Anicare Pharmaceuticals Pvt. Ltd.
Effective date: 2010-07-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:25:21

Label at a glance#

ProductVaporizing Chest Rub

Active ingredientCAMPHOR (SYNTHETIC), EUCALYPTUS OIL, MENTHOL

Label structure9 sections

Dosage and administration

See important warning under Children under 2 years of age, ask a doctor. Adults and children 2 years of age or older: Rub a thick layer on chest and throat. If desired, loosely cover with a soft dry cloth but keep clothing loose. Repeat up to 3 times daily, or as directed by a doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

DESCRIPTION SECTION

Camphor 4.7%

Menthol 1.0%

Eucalyptus Oil 1.0%

Purpose

DESCRIPTION SECTION

Cough suppressant, nasal decongestant & topical analgesic

Use:

INDICATIONS & USAGE SECTION

Temporarily relives symptoms associated with the common cold:

cough
nasal congestion
chest congestion

Temporarily relieves minor aches and pains of muscles.

Directions:

DOSAGE & ADMINISTRATION SECTION

See important warning under

“Do not use this product”

OTC - DO NOT USE SECTION

Children under 2 years of age, ask a doctor.
Adults and children 2 years of age or older: Rub a thick layer on chest and throat. If desired, loosely cover with a soft dry cloth but keep clothing loose.
Repeat up to 3 times daily, or as directed by a doctor.

Warnings:

WARNINGS SECTION

For external use only: Avoid contact with eyes

Ask a doctor before use if you have:

OTC - ASK DOCTOR SECTION

Chronic cough that lasts or as occurs with smoking, asthma or emphysema. Cough with excessive phlegm (mucus).

Do not use this product;

OTC - DO NOT USE SECTION

Near an open flame. By adding water. By mouth. In a microwave oven. On wounds or damaged skin. With tight bandages. In nostrils. Added to hot water or any container where you are heating water. May cause splattering and result in burns.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

Muscles aches and pains persist for more than 7 days or come back. Cough lasts more that 7 days comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition. If pregnant or breast-feeding, consult a physician before use

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical helps or contact a Poison Control Center immediately

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Petrolatum, Nutmeg Oil, Turpentine Oil, Cedar Leaf Oil, Thymol, Paraffin.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW!
FamilyCare
Chest Rub
VAPORIZING ACTION
Nasal Decongestant
Cough Suppressant
NET WT. 4 OZ
(113g)

Principal Display Panel FamilyCare Chest Rub

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1042788	camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Gel	PSN	1
1042788	camphor 0.047 MG/MG / Eucalyptus oil 0.01 MG/MG / menthol 0.01 MG/MG Topical Gel	SCD	1
1042788	camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52271-158-01	2020-01-31	C162847	48780-1	9d75b9d0-894d-f424-e053-dadaa90a57ce	Vaporizing Chest Rub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52271-158-01	Vaporizing Chest Rub	113 g in 1 JAR	GEL	113		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52271-158	VAPORIZING CHEST RUB (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [QUALITY CARE DISTRIBUTORS LLC]	1	Legacy NDC, 1 package rows	20100728_e7c84421-21e0-4620-b298-695723fc9d66.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	1
EUCALYPTUS OIL	ACTIVE INGREDIENT	2R04ONI662	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	1
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	1
EUCALYPTUS OIL	ACTIVE MOIETY	2R04ONI662	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	1
CEDAR LEAF OIL	INACTIVE INGREDIENT	BJ169U4NLG	1
NUTMEG OIL	INACTIVE INGREDIENT	Z1CLM48948	1
PARAFFIN	INACTIVE INGREDIENT	I9O0E3H2ZE	1
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	1
THYMOL	INACTIVE INGREDIENT	3J50XA376E	1
TURPENTINE	INACTIVE INGREDIENT	XJ6RUH0O4G	1

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Vaporizing Chest Rub
Menthol and Camphor and Eucalyptus Oil
CAMPHOR (SYNTHETIC)
EUCALYPTUS OIL
MENTHOL
PETROLATUM
PARAFFIN
NUTMEG OIL
TURPENTINE
THYMOL
CEDAR LEAF OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52271-158	52271-158-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CAMPHOR (SYNTHETIC)	5TJD82A1ET	ACTIB
EUCALYPTUS OIL	2R04ONI662	ACTIB
MENTHOL	L7T10EIP3A	ACTIB
PETROLATUM	4T6H12BN9U	IACT
PARAFFIN	I9O0E3H2ZE	IACT
NUTMEG OIL	Z1CLM48948	IACT
TURPENTINE	XJ6RUH0O4G	IACT
THYMOL	3J50XA376E	IACT
CEDAR LEAF OIL	BJ169U4NLG	IACT

Source Document#

Source XML

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 · 33 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
PARAFFIN	PARAFFIN	I9O0E3H2ZE	TABLET, EXTENDED RELEASE / ORAL		321 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	SPONGE / TOPICAL	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	TABLET, DELAYED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CAPSULE, EXTENDED RELEASE / ORAL	0.07 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CREAM, AUGMENTED / TOPICAL	26 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	CREAM / TOPICAL		300 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
NUTMEG OIL	NUTMEG OIL	Z1CLM48948	LIQUID / RESPIRATORY (INHALATION)	NA		Exact identifier — unii candidate 2 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	LOTION / TOPICAL	25 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	CAPSULE, EXTENDED RELEASE / ORAL		100 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	OINTMENT / TOPICAL		2860 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	TABLET / ORAL	0.7 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	EMULSION / TOPICAL	7.8 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	TABLET / ORAL	3.5 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	LIQUID / RESPIRATORY (INHALATION)	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	SUPPOSITORY / VAGINAL	27 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	SOAP / TOPICAL	0.85 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CREAM / TOPICAL		4213 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
THYMOL	THYMOL	3J50XA376E	LIQUID / RESPIRATORY (INHALATION)	0.01 %w/w		Exact identifier — unii candidate 2 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	TABLET, COATED / ORAL	0.07 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
NUTMEG OIL	NUTMEG OIL	Z1CLM48948	ELIXIR / ORAL	4.5 mg/5ml		Exact identifier — unii candidate 2 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	SUSPENSION / TOPICAL		11726 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	TABLET, EXTENDED RELEASE / ORAL	0.18 mg		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / TOPICAL		7275 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT, AUGMENTED / TOPICAL	81.94 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	AEROSOL, FOAM / TOPICAL		14235 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / OPHTHALMIC	88.4 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	SOAP / TOPICAL	0.4 %w/w		Exact identifier — unii candidate 11 equally ranked IID candidates
PARAFFIN	PARAFFIN	I9O0E3H2ZE	OINTMENT / RECTAL		38 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
THYMOL	THYMOL	3J50XA376E	POWDER, FOR SOLUTION / ORAL	NA		Exact identifier — unii candidate 2 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / AURICULAR (OTIC)	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	CAPSULE / VAGINAL	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	AEROSOL, FOAM / TOPICAL	7.9 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
PETROLATUM	PETROLATUM	4T6H12BN9U	OINTMENT / VAGINAL		4084 mg	Exact identifier — unii candidate 18 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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1f90ba87-1aa3-4099-996f-d0f8d0eb9193			e7c84421-21e0-4620-b298-695723fc9d66	2010-07-25	Warnings	Exact identifier spl id: 1f90ba87-1aa3-4099-996f-d0f8d0eb9193 spl set id: e7c84421-21e0-4620-b298-695723fc9d66

Reported adverse events (FAERS/openFDA)#

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