NDC 70784-005 Ato Pollen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70784-005?
What are the uses for Ato Pollen?
Which are Ato Pollen UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Ato Pollen 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)
- BEE POLLEN (UNII: 3729L8MA2C)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- ISOPENTYLDIOL (UNII: 19NOL5474Q)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
- PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- DIPENTAERYTHRITYL HEXAHYDROXYSTEARATE (UNII: 74J1X57U42)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- PEG-100 STEARATE (UNII: YD01N1999R)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LAURETH-7 (UNII: Z95S6G8201)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".