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  4. NDC Product Code: 60512-9080 Gas Relief Kids Relief

NDC 60512-9080 Gas Relief Kids Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 60512-9080?
  5. Gas Relief Kids Relief Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory .
NDC Product Code:
60512-9080
Proprietary Name:
Gas Relief Kids Relief
Product Type: [3]
Labeler Name: [5]
Homeolab Usa Inc
Labeler Code:
60512
Product Label ID:
1cce570b-5a0d-406e-8a0a-48fd7ee366ad
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
11-08-2010
End Marketing Date: [10]
05-07-2011
Listing Expiration Date: [11]
05-07-2011
Exclude Flag: [12]
D
Code Navigator:

Product Characteristics

Flavor(s):
RASPBERRY (C73413)
GRAPE (C73391)

Code Structure Chart

Product Details

What is NDC 60512-9080?

The NDC code 60512-9080 is assigned by the FDA to the product Gas Relief Kids Relief which is product labeled by Homeolab Usa Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60512-9080-8 1 bottle in 1 carton / 25 ml in 1 bottle. 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 Gas Relief Kids Relief?

Do not use more than directed.Take .75 ml orally at the onset of symptoms.Repeat every 15 minutes up to 4 times then reduce with improvement or as directed by a healthcare professional.Infants and children 0 to 9 years of age: .75 ml

Which are Gas Relief Kids Relief UNII Codes?

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

  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
  • DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8)
  • DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8) (Active Moiety)

Which are Gas Relief Kids Relief 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:

* 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.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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".