NDC 17856-0301 Hydrocodone Polistirex And Chlorpheniramine Polistirex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 17856-0301?
What are the uses for Hydrocodone Polistirex And Chlorpheniramine Polistirex?
Which are Hydrocodone Polistirex And Chlorpheniramine Polistirex UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCODONE (UNII: 6YKS4Y3WQ7)
- HYDROCODONE (UNII: 6YKS4Y3WQ7) (Active Moiety)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
Which are Hydrocodone Polistirex And Chlorpheniramine Polistirex 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:
- WATER (UNII: 059QF0KO0R)
- HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
- SUCROSE (UNII: C151H8M554)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CORN OIL (UNII: 8470G57WFM)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLCELLULOSE, UNSPECIFIED (UNII: 7Z8S9VYZ4B)
- SORBITOL (UNII: 506T60A25R)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
What is the NDC to RxNorm Crosswalk for Hydrocodone Polistirex And Chlorpheniramine Polistirex?
- RxCUI: 1087459 - HYDROcodone polistirex 10 MG / chlorpheniramine polistirex 8 MG in 5 mL 12HR Extended Release Oral Suspension
- RxCUI: 1087459 - 12 HR chlorpheniramine polistirex 1.6 MG/ML / hydrocodone polistirex 2 MG/ML Extended Release Suspension
- RxCUI: 1087459 - hydrocodone polistirex 10 MG / chlorpheniramine polistirex 8 MG per 5 ML 12HR Extended Release Oral Suspension
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Patient Education
Chlorpheniramine
Chlorpheniramine relieves red, itchy, watery eyes; sneezing; itchy nose or throat; and runny nose caused by allergies, hay fever, and the common cold. Chlorpheniramine helps control the symptoms of cold or allergies but will not treat the cause of the symptoms or speed recovery. Chlorpheniramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
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Hydrocodone Combination Products
Hydrocodone is available in combination with other ingredients, and different combination products are prescribed for different uses. Some hydrocodone combination products are used to relieve moderate-to-severe pain. Other hydrocodone combination products are used to relieve cough. Hydrocodone is in a class of medications called opiate (narcotic) analgesics and in a class of medications called antitussives. Hydrocodone relieves pain by changing the way the brain and nervous system respond to pain. Hydrocodone relieves cough by decreasing activity in the part of the brain that causes coughing. You will take hydrocodone in combination with at least one other medication, but this monograph only provides information about hydrocodone. Be sure to read information about the other ingredients in the hydrocodone product you are taking. Ask your doctor or pharmacist if you have any questions.
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[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".