NDC 66007-103 Ultra Cold Remedy Rapidmelts

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:
66007-103
Proprietary Name:
Ultra Cold Remedy Rapidmelts
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
66007
Start Marketing Date: [9]
02-06-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
15 MM
Imprint(s):
Z
Score:
1
Flavor(s):
CHERRY (C73375)

Code Structure Chart

Product Details

What is NDC 66007-103?

The NDC code 66007-103 is assigned by the FDA to the product Ultra Cold Remedy Rapidmelts which is product labeled by Izeen Pharma, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66007-103-18 1 bottle, plastic in 1 carton / 18 tablet in 1 bottle, plastic. 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 Ultra Cold Remedy Rapidmelts?

For best results, use at the first sign of a cold and continue to use until symptoms completely subsideadults and children 12 years of age and older:take 1 tablet at the onset of symptomsdissolve entire tablet in mouth. Do not chew. Do not swallow whole.repeat every 4-6 hours, not to exceed 4 tablets in 24 hoursto avoid minor stomach upset, do not take on an empty stomachdo not eat or drink for 15 minutes after use. Do not eat or drink citrus fruits or juices for 30 minutes before or after use. Otherwise, drink plenty of fluids.children under 12 years of age: ask a doctor before use

Which are Ultra Cold Remedy Rapidmelts UNII Codes?

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

Which are Ultra Cold Remedy Rapidmelts 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".