NDC 17856-0145 Infants Silapap
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-0145 - Infants Silapap
Product Characteristics
Product Packages
NDC Code 17856-0145-3
Package Description: 1 mL in 1 SYRINGE
Product Details
What is NDC 17856-0145?
What are the uses for Infants Silapap?
Which are Infants Silapap UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Infants Silapap 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Infants Silapap?
- RxCUI: 238159 - acetaminophen 500 MG in 5 mL Oral Solution
- RxCUI: 238159 - acetaminophen 100 MG/ML Oral Solution
- RxCUI: 238159 - acetaminophen 500 MG per 5 ML Oral Solution
- RxCUI: 238159 - acetaminophen 80 MG per 0.8 ML Oral Solution
- RxCUI: 238159 - APAP 100 MG/ML Oral Solution
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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".