FDA.reportPublic FDA data

Chestrub

Manufacturer
Delta Brands Inc | JELL PHARMACEUTICALS PVT LTD
Effective date
2024-12-17
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:44:15

Label at a glance#

ProductChestrub
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, EUCALYPTUS OIL
Label structure11 sections

Indications and uses

Temporarily relieves symptoms associated with the common cold: cough nasal congestion chest congestion Temporarily relieves minor aches and pains of muscles

Dosage and administration

See important warnings under "Do not Use this product" Children under 2 years of age, ask a doctor Adults and children 2 years of age and older: rub a thick layer on chest and throat. If desired loosely cover with a soft cloth but keep clothing loose. Repeat up to 3 times daily, or as directed by a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 4.7%

Menthol 1.0%

Eucalyptus Oil 1.0%

Purpose

OTC - PURPOSE SECTION

Cough Suppressant

Nasal Decongestant

Topical Anlagesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves 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 warnings under "Do not Use this product"

  • Children under 2 years of age, ask a doctor
  • Adults and children 2 years of age and older: rub a thick layer on chest and throat. If desired loosely cover with a soft 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 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

OTC - STOP USE SECTION

if Muscle aches and pains persist for more than 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 help or contact a Poison Control Center immediately.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1042786camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical OintmentPSN6
1042786camphor 0.047 MG/MG / Eucalyptus oil 0.01 MG/MG / menthol 0.01 MG/MG Topical OintmentSCD6
1042786camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical OintmentSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
20276-100-31Chestrub113 g in 1 JAROINTMENT1136

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
20276-100CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL) OINTMENT [DELTA BRANDS INC]6Current NDC, Legacy NDC, 1 package rows20241219_8e6f731f-c16a-41b2-9786-0cab588cfc8e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ET3
EUCALYPTUS OILACTIVE INGREDIENT2R04ONI6623
MENTHOLACTIVE INGREDIENTL7T10EIP3A3
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ET3
EUCALYPTUS OILACTIVE MOIETY2R04ONI6623
MENTHOLACTIVE MOIETYL7T10EIP3A3
CEDAR LEAF OILINACTIVE INGREDIENTBJ169U4NLG3
NUTMEGINACTIVE INGREDIENTAEE24M3MQ93
PARAFFININACTIVE INGREDIENTI9O0E3H2ZE3
PETROLATUMINACTIVE INGREDIENT4T6H12BN9U3
THYMOLINACTIVE INGREDIENT3J50XA376E3
TURPENTINEINACTIVE INGREDIENTXJ6RUH0O4G3

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-10020276-100-31

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
NameUNIIKind
CEDAR LEAF OILBJ169U4NLGIACT
NUTMEGAEE24M3MQ9IACT
PARAFFINI9O0E3H2ZEIACT
PETROLATUM4T6H12BN9UIACT
THYMOL3J50XA376EIACT
TURPENTINEXJ6RUH0O4GIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
MENTHOLL7T10EIP3AACTIB
EUCALYPTUS OIL2R04ONI662ACTIB

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 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
THYMOLTHYMOL3J50XA376ELIQUID / RESPIRATORY (INHALATION)0.01 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZEOINTMENT / TOPICAL2860 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZEOINTMENT / TOPICAL2860 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
THYMOLTHYMOL3J50XA376ELIQUID / RESPIRATORY (INHALATION)0.01 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
THYMOLTHYMOL3J50XA376EPOWDER, FOR SOLUTION / ORALNAExact identifier — unii candidate
4 equally ranked IID candidates
THYMOLTHYMOL3J50XA376EPOWDER, FOR SOLUTION / ORALNAExact identifier — unii candidate
4 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
2 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
ChestrubCAMPHOR MENTHOL EUCALYPTUS OILDelta Brands Inc8e6f731f-c16a-41b2-9786-0cab588cfc8e2024-12-17WarningsExact identifier
ndc (package): 20276-100-31
ndc (product): 20276-100
ndc11 (package): 20276010031
spl id: 29740204-fdf3-705b-e063-6294a90a0acf
spl set id: 8e6f731f-c16a-41b2-9786-0cab588cfc8e

Reported adverse events (FAERS/openFDA)#

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