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  4. NDC Product Code: 17856-6833 Mi Acid

NDC 17856-6833 Mi Acid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 17856-6833?
  5. Mi Acid Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
17856-6833
Proprietary Name:
Mi Acid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Atlantic Biologicals Corp.
Labeler Code:
17856
Product Label ID:
414198a7-ac04-4fc8-a271-18e9fccd38d1
Start Marketing Date: [9]
12-28-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - OPAQUE)
Flavor(s):
MINT (C73404)
LEMON (C73396)

Code Structure Chart

Product Details

What is NDC 17856-6833?

The NDC code 17856-6833 is assigned by the FDA to the product Mi Acid which is product labeled by Atlantic Biologicals Corp.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 17856-6833-1 50 cup, unit-dose in 1 box, unit-dose / 30 ml in 1 cup, unit-dose. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Mi Acid?

•shake well before use•measure with dosing cup provided•adults and children 12 years and over: 10 mL – 20 mL between meals, at bedtime or as directed by a doctor•do not take more than 120 mL in any 24 hour period•do not use the maximum dosage for more than 2 weeks•children under 12 years: ask a doctor•mL = milliliter

Which are Mi Acid UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Mi Acid Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Mi Acid?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 210036 - Mi-Acid 200 MG / 200 MG / 20 MG in 5 mL Oral Suspension
  • RxCUI: 210036 - aluminum hydroxide 40 MG/ML / magnesium hydroxide 40 MG/ML / simethicone 4 MG/ML Oral Suspension [Mi-Acid]
  • RxCUI: 210036 - Mi-Acid (aluminum hydroxide 200 MG / magnesium hydroxide 200 MG / simethicone 20 MG) per 5 ML Oral Suspension
  • RxCUI: 210036 - Mi-Acid (aluminum hydroxide 40 MG / magnesium hydroxide 40 MG / simethicone 4 MG) per ML Oral Suspension
  • RxCUI: 210036 - Mi-Acid (aluminum hydroxide 400 MG / magnesium hydroxide 400 MG / simethicone 40 MG) per 10 ML Oral Suspension

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".