curetech Chest Rub

Manufacturer: Curetech Skincare
Effective date: 2021-09-28
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:42:32

Label at a glance#

Productcuretech Chest Rub

Active ingredientCAMPHOR (SYNTHETIC), EUCALYPTUS OIL, MENTHOL

Label structure8 sections

Indications and uses

when applied to chest and throat, temporarily relieves cough due to minor throat and bronchial irritation associated with the common cold when applied to muscles and joints, temporarily relieves 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 over rub a thick layer on throat & chest & cover with a warm, dry cloth if desired keep clothing loose about throat and chest to help vapors reach the nose and mouth use up to three times daily or as directed by doctor for muscle/joint minor aches and pains apply to affected area not more than 3 to 4 times daily children under...

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 4.7%

Menthol 1.25%

Eucalyptus oil 1.2%

Purpose

OTC - PURPOSE SECTION

Cough suppressant & Topical Analgesic

Cough suppressant

Cough suppressant & Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

when applied to chest and throat, temporarily relieves cough due to minor throat and bronchial irritation associated with the common cold
when applied to muscles and joints, temporarily relieves 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
with tight bandages
in nostrils
on wounds or damaged skin

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

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

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 persist more than 7 days or come back
cough lasts for more than 7 days, comes back, or occurs with 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 over
rub a thick layer on throat & chest &
cover with a warm, dry cloth if desired
keep clothing loose about throat and chest to help vapors reach the nose and mouth
use up to three times daily or as directed by doctor
for muscle/joint minor aches and pains apply to affected area not more than 3 to 4 times daily
children under 2 years: do not use

Other information

STORAGE AND HANDLING SECTION

store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

cedar leaf oil, methylparaben, nutmeg oil, petrolatum, propylparaben, thymol, turpentine oil

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Fact and PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2003749	camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical Ointment	PSN	1
2003749	camphor 0.047 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.0125 MG/MG Topical Ointment	SCD	1
2003749	camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical Ointment	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73622-3022-1	2023-01-30	C162847	48780-1	f386c64a-028b-0266-e053-dadaa90a7c1a	Curetech ChestRub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73622-3022-1	curetech Chest Rub	113 g in 1 JAR	OINTMENT	113		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73622-3022	CURETECH CHEST RUB (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [CURETECH SKINCARE]	1	Legacy NDC, 1 package rows	20210930_cd16e910-908a-309f-e053-2a95a90a0a25.zip

Products#

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

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

curetech Chest Rub
Camphor (synthetic), Eucalyptus oil, and Menthol
CEDAR LEAF OIL
NUTMEG OIL
THYMOL
TURPENTINE OIL
PETROLATUM
METHYLPARABEN
PROPYLPARABEN
CAMPHOR (SYNTHETIC)
EUCALYPTUS OIL
MENTHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73622-3022	73622-3022-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CEDAR LEAF OIL	BJ169U4NLG	IACT
NUTMEG OIL	Z1CLM48948	IACT
THYMOL	3J50XA376E	IACT
TURPENTINE OIL	C5H0QJ6V7F	IACT
PETROLATUM	4T6H12BN9U	IACT
METHYLPARABEN	A2I8C7HI9T	IACT
PROPYLPARABEN	Z8IX2SC1OH	IACT
CAMPHOR (SYNTHETIC)	5TJD82A1ET	ACTIB
EUCALYPTUS OIL	2R04ONI662	ACTIB
MENTHOL	L7T10EIP3A	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
cd16ebd8-f611-d283-e053-2995a90ad785			cd16e910-908a-309f-e053-2a95a90a0a25	2021-09-28	Warnings	Exact identifier spl id: cd16ebd8-f611-d283-e053-2995a90ad785 spl set id: cd16e910-908a-309f-e053-2a95a90a0a25

Reported adverse events (FAERS/openFDA)#

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