NDC 60709-100 Nano Ppc
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 60709-100?
What are the uses for Nano Ppc?
Which are Nano Ppc UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAFFEINE (UNII: 3G6A5W338E)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
Which are Nano Ppc 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- OLEA EUROPAEA FRUIT VOLATILE OIL (UNII: 8E7358CX1J)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM LAUROYL GLUTAMATE (UNII: NCX1UU2D33)
- CARBOMER 1342 (UNII: 809Y72KV36)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SOYBEAN OIL (UNII: 241ATL177A)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- EPIGALLOCATECHIN GALLATE (UNII: BQM438CTEL)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- LEVOCARNITINE (UNII: 0G389FZZ9M)
* 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".