Earths Best Cold Relief Vapor
- Manufacturer
- The Hain Celestial Group, Inc
- Effective date
- 2012-05-23
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:32:05
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Camphor 5.3%
Menthol 2.8%
Eucalyptus Globulus Leaf Oil 1.3%
OTC - PURPOSE SECTION
Natural Skin Protectant
INDICATIONS & USAGE SECTION
- Temporarily relieves cough due to common cold
- On muscles and joints, temporarily relieves minor aches and pains
WARNINGS SECTION
For external use only. Avoid contact with eyes. Do not take by mouth or place in nostrils. Ask a doctor before use if you have cough with too much phlegm (mucus)or persistent or chronic cough such asthma. When using this product do not heat, microwave, add to hot water or any container where heating water. May cause splattering and result in burns. Stop use and ask doctor if muscle aches and pains persist more than 7days or come back,cough lasts more than 1 week, comes back or occurs with fiver, rash or persistent headache. There could be signs of serious condition. If pregnant or breastfeeding, 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 Poison Center right away.
DOSAGE & ADMINISTRATION SECTION
- Rub over chest and throat in a thick layer or rub on aching muscles.
- Cover with warm dry cloth if desired.
- Keep clothing loose around chest and throat to help vapors to reach nose and mouth.
- Use up to 3 times per day or as directed by doctor. Children under 2 years of age : Ask a doctor.
INACTIVE INGREDIENT SECTION
Helianthus Annuus (Sunflower) Seed Oil *, Beeswax*, Mentha Piperita (Peppermint) Oil*
OTC - QUESTIONS SECTION
Questions? Visit
www.earthsbest.com or call 877-527-6801
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1297310 | camphor 5.3 % / eucalyptus oil 1.3 % / menthol 2.8 % Topical Ointment | PSN | 1 |
| 1297310 | camphor 0.053 MG/MG / Eucalyptus oil 0.013 MG/MG / menthol 0.028 MG/MG Topical Ointment | SCD | 1 |
| 1297310 | camphor 5.3 % / eucalyptus oil 1.3 % / menthol 2.8 % Topical Ointment | SY | 1 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 61995-0758-2 | 2019-11-13 | C162847 | 48780-1 | 97449f38-c2e7-f6ea-e053-dbdaa90aa703 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61995-0758-2 | Earths Best Cold Relief Vapor | 80 g in 1 JAR | OINTMENT | 80 | 1 | |
| 61995-0758-2 | Earths Best Cold Relief Vapor | 1 in 1 CARTON | OINTMENT | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 61995-0758 | EARTHS BEST COLD RELIEF VAPOR (CAMPHOR, MENTHOL, EUCALYPTUS GLOBULUS LEAF OIL) OINTMENT [THE HAIN CELESTIAL GROUP, INC] | 1 | Legacy NDC, 2 package rows | 20120525_8f8beee0-8a27-4b31-90b9-9d3066dc67fe.zip |
DailyMed Socrata Ingredients#
| 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 | |
| PEPPERMINT OIL | INACTIVE INGREDIENT | AV092KU4JH | 1 | |
| SUNFLOWER OIL | INACTIVE INGREDIENT | 3W1JG795YI | 1 | |
| YELLOW WAX | INACTIVE INGREDIENT | 2ZA36H0S2V | 1 |
Products#
Every source-derived product name is available through these pages.
- Earths Best Cold Relief Vapor
- Camphor, Menthol, Eucalyptus Globulus Leaf Oil
- CAMPHOR (NATURAL)
- SUNFLOWER OIL
- YELLOW WAX
- PEPPERMINT OIL
- MENTHOL
- EUCALYPTUS OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 61995-0758 | 61995-0758-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CAMPHOR (NATURAL) | N20HL7Q941 | ACTIB |
| SUNFLOWER OIL | 3W1JG795YI | IACT |
| YELLOW WAX | 2ZA36H0S2V | IACT |
| PEPPERMINT OIL | AV092KU4JH | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
| EUCALYPTUS OIL | 2R04ONI662 | ACTIB |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SPRAY, METERED / SUBLINGUAL | 1 mg | ||
| YELLOW WAX | YELLOW WAX | 2ZA36H0S2V | TABLET, DELAYED RELEASE / ORAL | 0.1 mg | ||
| YELLOW WAX | YELLOW WAX | 2ZA36H0S2V | CAPSULE, EXTENDED RELEASE / ORAL | 80.67 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | OINTMENT / TOPICAL | 0.2 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | GUM, CHEWING / BUCCAL | 526 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | FILM / BUCCAL | 12 mg | ||
| YELLOW WAX | YELLOW WAX | 2ZA36H0S2V | TABLET, EXTENDED RELEASE / ORAL | 0.01 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | TABLET / SUBLINGUAL | 0.15 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | TABLET / ORAL | 28 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | TABLET, ORALLY DISINTEGRATING / ORAL | 3 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | FILM, SOLUBLE / BUCCAL | 3 mg | ||
| YELLOW WAX | YELLOW WAX | 2ZA36H0S2V | TABLET / ORAL | 3.22 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SHAMPOO / TOPICAL | 0.2 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | PASTE, DENTIFRICE / DENTAL | 49.3 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SOLUTION / DENTAL | 0.04 %v/v | ||
| YELLOW WAX | YELLOW WAX | 2ZA36H0S2V | OINTMENT / TOPICAL | 20 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | ELIXIR / ORAL | 0.04 mg/1ml | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | CAPSULE / ORAL | 60 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SUSPENSION / ORAL | 100 mg/1ml | ||
| YELLOW WAX | YELLOW WAX | 2ZA36H0S2V | CAPSULE / ORAL | 44 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | LOZENGE / ORAL | 12 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | POWDER / SUBLINGUAL | 1 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | CONCENTRATE / ORAL | 0.05 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SOLUTION / ORAL | 53 mg | ||
| YELLOW WAX | YELLOW WAX | 2ZA36H0S2V | TABLET, COATED / ORAL | 213.7 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SYRUP / ORAL | 120 mg | ||
| YELLOW WAX | YELLOW WAX | 2ZA36H0S2V | CREAM / TOPICAL | 5 %w/w | ||
| YELLOW WAX | YELLOW WAX | 2ZA36H0S2V | TABLET, SUGAR COATED / ORAL | NA | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | GUM, CHEWING / ORAL | 526 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | POWDER, DENTIFRICE / DENTAL | NA |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| de6c79e0-dfe2-4e13-9edf-0b0c3703a7f4 | 8f8beee0-8a27-4b31-90b9-9d3066dc67fe | 2012-05-23 | Warnings | de6c79e0-dfe2-4e13-9edf-0b0c3703a7f4 8f8beee0-8a27-4b31-90b9-9d3066dc67fe |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

