FDA.reportPublic FDA data

Walgreens Lavender Chest Rub

Manufacturer
Walgreen Company
Effective date
2026-03-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:51:17

Label at a glance#

ProductWalgreens Lavender Chest Rub
Active ingredientCAMPHOR (NATURAL), MENTHOL, EUCALYPTUS OIL
Label structure9 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 warning under "When using this product" adults and children 2 years and over: for cough suppression rub a thick layer on the throat and chest for cough 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 3 times daily or as directed by a doctor for muscle/joint minor aches and pains apply to affected area not more than 3...

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

Camphor – Cough suppressant/topical analgesic
Eucalyptus oil – Cough suppressant
Menthol – 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

Do not use

OTC - DO NOT USE SECTION

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

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional 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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

see important warning under "When using this product"

  • adults and children 2 years and over:
  • for cough suppression
  • rub a thick layer on the throat and chest for cough
  • 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 3 times daily or as directed by a doctor
  • for muscle/joint minor aches and pains apply to affected area not more than 3 to 4 times daily
  • children under 2 years: ask a doctor

Other Information

OTHER SAFETY INFORMATION

  • store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

cetostearyl alcohol, fragrance, thymol, titanium dioxide, turpentine oil, white petrolatum

Questions?

OTC - QUESTIONS SECTION

Call 1-800-925-4733

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image 1Image 1Package Label Principal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
200293camphor 4.7 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical OintmentPSN3
200293camphor 0.047 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical OintmentSCD3
200293camphor 4.7 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical OintmentSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130311917009469GTIN-13: 0311917009469
EAN-13: 0311917009469
GTIN-12: 311917009469
UPC-A: 311917009469
GTIN storage (14 digits): 00311917009469		Walgreens Lavender Chest Rub.jpg
Data codeITF551002Walgreens Lavender Chest Rub.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-9802-01Walgreens Lavender Chest Rub50 g in 1 JAROINTMENT503
0363-9802-01Walgreens Lavender Chest Rub1 in 1 CARTONOINTMENT13

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
0363-98020363-9802-01

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
NameUNIIKind
CAMPHOR (NATURAL)N20HL7Q941ACTIB
WHITE PETROLATUMB6E5W8RQJ4IACT
FRAGRANCE 135765EM498GW35IACT
THYMOL3J50XA376EIACT
TURPENTINE OILC5H0QJ6V7FIACT
MENTHOLL7T10EIP3AACTIB
EUCALYPTUS OIL2R04ONI662ACTIB
CETOSTEARYL ALCOHOL2DMT128M1SIACT
TITANIUM DIOXIDE15FIX9V2JPIACT

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
Walgreens Lavender Chest RubCAMPHOR, EUCALYPTUS OIL, MENTHOLWalgreen Company327a1a00-852d-2756-e063-6394a90a5e292026-03-25WarningsExact identifier
ndc (package): 0363-9802-01
ndc (product): 0363-9802
ndc11 (package): 00363980201
spl id: 4dd2d30d-e40c-5432-e063-6394a90aaa53
spl set id: 327a1a00-852d-2756-e063-6394a90a5e29

Reported adverse events (FAERS/openFDA)#

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