Bactimicina Vapor Rub Ointment
NDC Package 24286-1580-2
Package Information
Bactimicina Vapor Rub (vapor rub) ointment is see important warnings under "When using this product"•adult and children 2 years and over:For cough suppression •rub a thick layer on throat and chest •cover with a warm, dry cloth if desired •clothing should be loose about throat and chest to help vapors reach the nose and mouth•Use up to three times daily or as directed by a doctorFor minor aches and pains of muscles and joints •apply to affected area not more than 3 to 4 times dailyChildren under 2 years: do not use. This formulation utilizes a ointment delivery system. Marketed by Dlc Laboratories, Inc., this product is identified by NDC 24286-1580 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Ointment
- RxCUI: 727137 - camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical Ointment
- RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Chest Rub
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 24286 - Dlc Laboratories, Inc.
- 24286-1580 - Bactimicina Vapor Rub
- 24286-1580-2 - 1 JAR in 1 BOX / 56.7 g in 1 JAR
- 24286-1580 - Bactimicina Vapor Rub
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 24286-1580-2 identifies a specific commercial package of 1 jar in 1 box / 56.7 g in 1 jar of Bactimicina Vapor Rub, a human over the counter drug labeled by Dlc Laboratories, Inc.. This ointment is formulated for topical use and contains camphor (synthetic); 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 Dlc Laboratories, Inc. on March 28, 2024. The current certification is valid through December 31, 2027.
How is this Dlc Laboratories, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 24286158002. 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.