Mentholatum Soothing Vapor Rub Lavender Ointment
NDC Package 10742-1060-1
Package Information
Mentholatum Soothing Vapor Rub Lavender (camphor, eucalyptus oil, menthol) ointment is see important warnings under "When using this product"adults and children 2 years and over:rub a thick layer on the throat and chest for cough, or rub on sore, aching muscles or jointscover with a warm, dry cloth if desiredclothing should be left loose about the throat and chest to help vapors reach the nose and mouthuse up to 3 times daily, or as directed by a doctorchildren under 2 years of age: Ask a doctor. This formulation utilizes a ointment delivery system. Marketed by The Mentholatum Company, this product is identified by NDC 10742-1060 and is authorized under FDA application M017.
Identification & Billing
- RxCUI: 1297310 - camphor 5.3 % / eucalyptus oil 1.3 % / menthol 2.8 % Topical Ointment
- RxCUI: 1297310 - camphor 0.053 MG/MG / Eucalyptus oil 0.013 MG/MG / menthol 0.028 MG/MG Topical Ointment
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 10742 - The Mentholatum Company
- 10742-1060 - Mentholatum Soothing Vapor Rub Lavender
- 10742-1060-1 - 1 JAR in 1 CARTON / 28 g in 1 JAR
- 10742-1060 - Mentholatum Soothing Vapor Rub Lavender
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 10742-1060-1 identifies a specific commercial package of 1 jar in 1 carton / 28 g in 1 jar of Mentholatum Soothing Vapor Rub Lavender, a human over the counter drug labeled by The Mentholatum Company. This ointment is formulated for topical use and contains camphor, (-)-; eucalyptus oil; menthol as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by The Mentholatum Company on August 15, 2025. The current certification is valid through December 31, 2027.
How is this The Mentholatum Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 10742106001. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.