NDC Package 27854-115-01 Melox

Aluminum Hydroxide,Magnesium Hydroxide,Simethicone Suspension Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
27854-115-01
Package Description:
355 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Melox
Non-Proprietary Name:
Aluminum Hydroxide, Magnesium Hydroxide, Simethicone
Substance Name:
Aluminum Hydroxide; Dimethicone; Magnesium Hydroxide
Usage Information:
• shake well before each use• adults and children 12 years and older: take 2 to 4 teaspoonfuls between meals, at bedtime, or as directed by a doctor• do not exceed 16 teaspoonfuls in a 24 hour period or use the maximum dosage for more than 2 weeks• children under 12: ask a doctor
11-Digit NDC Billing Format:
27854011501
NDC to RxNorm Crosswalk:
  • RxCUI: 307746 - aluminum hydroxide 200 MG / magnesium hydroxide 200 MG / simethicone 20 MG in 5 mL Oral Suspension
  • RxCUI: 307746 - aluminum hydroxide 40 MG/ML / magnesium hydroxide 40 MG/ML / simethicone 4 MG/ML Oral Suspension
  • RxCUI: 307746 - aluminum hydroxide 1200 MG / milk of magnesia 1200 MG / dimethicone 120 MG per 30 ML Oral Suspension
  • RxCUI: 307746 - aluminum hydroxide 200 MG / milk of magnesia 200 MG / dimethicone 20 MG per 5 ML Oral Suspension
  • RxCUI: 307746 - aluminum hydroxide 400 MG / milk of magnesia 400 MG / dimethicone 40 MG per 10 ML Oral Suspension
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Belmora Llc
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    part331
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-01-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 27854-115-01?

    The NDC Packaged Code 27854-115-01 is assigned to a package of 355 ml in 1 bottle of Melox, a human over the counter drug labeled by Belmora Llc. The product's dosage form is suspension and is administered via oral form.

    Is NDC 27854-115 included in the NDC Directory?

    Yes, Melox with product code 27854-115 is active and included in the NDC Directory. The product was first marketed by Belmora Llc on June 01, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 27854-115-01?

    The 11-digit format is 27854011501. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-227854-115-015-4-227854-0115-01