Calorub
- Manufacturer
- The Mentholatum Company
- Effective date
- 2018-07-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:56:07
Label at a glance#
ProductCalorub
Active ingredientMENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10742-2120-1 | Calorub | 35 g in 1 TUBE | CREAM | 35 | 1 | |
| 10742-2120-1 | Calorub | 1 in 1 CARTON | CREAM | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10742-2120 | CALORUB (MENTHOL, METHYL SALICYLATE) CREAM [THE MENTHOLATUM COMPANY] | 1 | 2 package rows | 20180702_7d894fd0-8066-4747-b7f8-bfefd9d665f0.zip |
Products#
Every source-derived product name is available through these pages.
- Calorub
- Menthol, Methyl salicylate
- MENTHOL, UNSPECIFIED FORM
- MENTHOL
- METHYL SALICYLATE
- SALICYLIC ACID
- CETOSTEARYL ALCOHOL
- EUCALYPTUS OIL
- LANOLIN
- LIGHT MINERAL OIL
- PROPYLENE GLYCOL
- WATER
- QUATERNIUM-15
- SODIUM CETOSTEARYL SULFATE
- TURPENTINE OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10742-2120 | 10742-2120-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL, UNSPECIFIED FORM | L7T10EIP3A | ACTIB |
| METHYL SALICYLATE | LAV5U5022Y | ACTIB |
| CETOSTEARYL ALCOHOL | 2DMT128M1S | IACT |
| EUCALYPTUS OIL | 2R04ONI662 | IACT |
| LANOLIN | 7EV65EAW6H | IACT |
| LIGHT MINERAL OIL | N6K5787QVP | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| WATER | 059QF0KO0R | IACT |
| QUATERNIUM-15 | E40U03LEM0 | IACT |
| SODIUM CETOSTEARYL SULFATE | 7ZBS06BH4B | IACT |
| TURPENTINE OIL | C5H0QJ6V7F | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 7d894fd0-8066-4747-b7f8-bfefd9d665f0 | 7d894fd0-8066-4747-b7f8-bfefd9d665f0 | 2018-07-02 | 7d894fd0-8066-4747-b7f8-bfefd9d665f0 7d894fd0-8066-4747-b7f8-bfefd9d665f0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
