NDC 61941-1002 Kids-eeze Chest Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 61941-1002?
What are the uses for Kids-eeze Chest Relief?
Which are Kids-eeze Chest Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Kids-eeze Chest 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- ETHYLCELLULOSE (4 MPA.S) (UNII: KC5472WRJK)
- ETHYLENE GLYCOL (UNII: FC72KVT52F)
- MALIC ACID (UNII: 817L1N4CKP)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2) (UNII: 5KY68S2577)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Kids-eeze Chest Relief?
- RxCUI: 1111099 - Kids-Eeze Chest Relief 100 MG Chewable Tablet
- RxCUI: 1111099 - guaifenesin 100 MG Chewable Tablet [Kids-Eeze Chest Relief]
- RxCUI: 866449 - guaiFENesin 100 MG Chewable Tablet
- RxCUI: 866449 - guaifenesin 100 MG Chewable Tablet
* Please review the disclaimer below.
[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".