NDC 21695-705 Cough
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-705 - Cough
Product Characteristics
Product Packages
NDC Code 21695-705-04
Package Description: 118 mL in 1 BOTTLE
Product Details
What is NDC 21695-705?
What are the uses for Cough?
Which are Cough UNII Codes?
The UNII codes for the active ingredients in this product are:
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Cough 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:
- CARAMEL (UNII: T9D99G2B1R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CORN SYRUP (UNII: 9G5L16BK6N)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- MENTHOL (UNII: L7T10EIP3A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Cough?
- RxCUI: 310604 - guaiFENesin 100 MG in 5 mL Oral Solution
- RxCUI: 310604 - guaifenesin 20 MG/ML Oral Solution
- RxCUI: 310604 - guaifenesin 100 MG per 5 ML Oral Solution
- RxCUI: 310604 - guaifenesin 100 MG per 5 ML Oral Syrup
- RxCUI: 310604 - guaifenesin 200 MG per 10 ML Oral Solution
* 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".