NDC 63922-601 999 Ganmaoling Cold

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:
63922-601
Proprietary Name:
999 Ganmaoling Cold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kingsway
Labeler Code:
63922
Start Marketing Date: [9]
07-30-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - CLEAR)
Shape:
CAPSULE (C48336)
Size(s):
20 MM
Score:
2

Product Packages

NDC Code 63922-601-01

Package Description: 1 BLISTER PACK in 1 BOX / 12 CAPSULE in 1 BLISTER PACK (63922-601-12)

Product Details

What is NDC 63922-601?

The NDC code 63922-601 is assigned by the FDA to the product 999 Ganmaoling Cold which is product labeled by Kingsway. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63922-601-01 1 blister pack in 1 box / 12 capsule in 1 blister pack (63922-601-12). 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 999 Ganmaoling Cold?

Uses  Temporarily relieves the following symptoms associated with the common cold, hay fever or other upper respiratory allergies: • Minor aches an pains • Headache •Sneezing • Muscular aches • Itchy, watery eyes • Runny nose • Sore Throat • Itching of the nose or throat • Fever

Which are 999 Ganmaoling Cold UNII Codes?

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

Which are 999 Ganmaoling Cold 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 999 Ganmaoling Cold?

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: 1303251 - acetaminophen 100 MG / caffeine 2 MG / chlorpheniramine maleate 2 MG Oral Capsule
  • RxCUI: 1303251 - APAP 100 MG / Caffeine 2 MG / Chlorpheniramine Maleate 2 MG Oral Capsule

* 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".