NDC 60512-6001 Asthma Respiratory Care Real Relief

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
60512-6001
Proprietary Name:
Asthma Respiratory Care Real Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Homeolab Usa Inc.
Labeler Code:
60512
Start Marketing Date: [9]
07-25-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
8 MM
Score:
1

Product Packages

NDC Code 60512-6001-0

Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE

Product Details

What is NDC 60512-6001?

The NDC code 60512-6001 is assigned by the FDA to the product Asthma Respiratory Care Real 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 60512-6001-0 90 tablet, chewable 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 Asthma Respiratory Care Real Relief?

Chew tablets and let dissolve in mouth.Do not use more than directed.Do not take with food.Repeat 4 times daily and reduce intake with improvement or as directed by a health professional. Age DoseAdults and children 12 years of age and older2 tabletsChildren 2 to 11 years of age1 tabletChildren under 2 years of ageAsk a doctor

Which are Asthma Respiratory Care Real Relief UNII Codes?

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

Which are Asthma Respiratory Care Real 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:

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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".