Indications and uses
on chest and throat, temporarily relieves cough due to common cold on muscles and jonts, temporarily releives minor aches and pains
on chest and throat, temporarily relieves cough due to common cold on muscles and jonts, temporarily releives minor aches and pains
See imporatant warning under "When using this product" adults + children 2 yrs + over: rub a thick layer on chest + throat or rub on sore aching muscles cover with warm, dry cloth if desired keep clothing loose about throat/chest to help vapors reach the nose/mouth repeat up to three times per 24 hours or as directed by doctor children under 2 years of age: ask a doctor
Camphor 4.8%
Eucalyptus oil 1.2%
Menthol 2.6%
cough suppressant + topical analgesic
For external use only; avoid contact with eyes
If you have
Do not
These could be signs of a serious condition
ask a health professional before use.
In case of accidental ingestion, get medical help or contact a Poison Control Center right away.
See imporatant warning under "When using this product"
store at room temperature
cedarleaf oil, mutmeg oil, special petrolaturm, spirits of trupentine, thymol
Call 1-888-593-0593
FALIURE TO FOLLOW THSE WARNINGS COULD RESULT IN SERIOUS CONSEQUENCES
Walgreens Pharmacist survey Study, November 2012
*This product is not manufactured or distributed by Procter + Gamble, the distributor of Vicks VapoRub
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com
The active ingredients in Chest Rub work naturally to relieve coughing due to colds when you brath in the medicated vapors. Chest Rub also relieves minor muscles aches and pains
Well at Walgreens
WALGREENS PHARMACIST RECOMMENDED
Chest Rub
Cough Suppressant/Topical Analgesic
Compare to Vicks VapoRub active ingredients
NET WT 3.53 oz (100 g)
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| CAMPHOR (NATURAL) | ACTIVE INGREDIENT | N20HL7Q941 | 1 | |
| EUCALYPTUS OIL | ACTIVE INGREDIENT | 2R04ONI662 | 1 | |
| MENTHOL | ACTIVE INGREDIENT | L7T10EIP3A | 1 | |
| CAMPHOR (NATURAL) | ACTIVE MOIETY | N20HL7Q941 | 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 OIL | INACTIVE INGREDIENT | C5H0QJ6V7F | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 0363-0248 | 0363-0248-75 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CAMPHOR (NATURAL) | N20HL7Q941 | ACTIB |
| EUCALYPTUS OIL | 2R04ONI662 | ACTIB |
| MENTHOL | L7T10EIP3A | ACTIB |
| CEDAR LEAF OIL | BJ169U4NLG | IACT |
| NUTMEG OIL | Z1CLM48948 | IACT |
| PETROLATUM | 4T6H12BN9U | IACT |
| PARAFFIN | I9O0E3H2ZE | IACT |
| TURPENTINE OIL | C5H0QJ6V7F | IACT |
| THYMOL | 3J50XA376E | IACT |
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | TABLET, COATED / ORAL | 0.07 mg | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | CREAM, AUGMENTED / TOPICAL | 26 %w/w | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | SUPPOSITORY / VAGINAL | 27 mg | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | CREAM / TOPICAL | 300 mg | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | OINTMENT / TOPICAL | 2860 mg | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | OINTMENT / RECTAL | 38 mg | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | SOAP / TOPICAL | 0.4 %w/w | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | OINTMENT / AURICULAR (OTIC) | NA | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | OINTMENT / VAGINAL | 4084 mg | ||
| THYMOL | THYMOL | 3J50XA376E | POWDER, FOR SOLUTION / ORAL | NA | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | CAPSULE / VAGINAL | NA | ||
| NUTMEG OIL | NUTMEG OIL | Z1CLM48948 | LIQUID / RESPIRATORY (INHALATION) | NA | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | LOTION / TOPICAL | 25 %w/w | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | AEROSOL, FOAM / TOPICAL | 14235 mg | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | TABLET / ORAL | 3.5 mg | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | CAPSULE, EXTENDED RELEASE / ORAL | 0.07 mg | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | CREAM / TOPICAL | 4213 mg | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | TABLET, EXTENDED RELEASE / ORAL | 0.18 mg | ||
| THYMOL | THYMOL | 3J50XA376E | LIQUID / RESPIRATORY (INHALATION) | 0.01 %w/w | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | AEROSOL, FOAM / TOPICAL | 7.9 %w/w | ||
| NUTMEG OIL | NUTMEG OIL | Z1CLM48948 | ELIXIR / ORAL | 4.5 mg/5ml | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | EMULSION / TOPICAL | 7.8 %w/w | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | TABLET / ORAL | 0.7 mg | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | TABLET, DELAYED RELEASE / ORAL | 0.2 mg | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | OINTMENT, AUGMENTED / TOPICAL | 81.94 %w/w | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | TABLET, EXTENDED RELEASE / ORAL | 321 mg | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | LIQUID / RESPIRATORY (INHALATION) | NA | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | OINTMENT / TOPICAL | 7275 mg | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | SUSPENSION / TOPICAL | 11726 mg | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | SPONGE / TOPICAL | NA | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | OINTMENT / OPHTHALMIC | 88.4 %w/w | ||
| PETROLATUM | PETROLATUM | 4T6H12BN9U | SOAP / TOPICAL | 0.85 %w/w | ||
| PARAFFIN | PARAFFIN | I9O0E3H2ZE | CAPSULE, EXTENDED RELEASE / ORAL | 100 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| c73f547a-9ad2-46b6-b677-5cbe84f94188 | f537e999-66fc-4504-9b4a-3ca80c02a27c | 2020-04-29 | Warnings | f537e999-66fc-4504-9b4a-3ca80c02a27c |
Adverse event summaries are temporarily unavailable. Other product information remains available.