NDC 82408-301 Delay Sprays For External-use
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 82408-301?
What are the uses for Delay Sprays For External-use?
Which are Delay Sprays For External-use UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPIMEDIUM BREVICORNU WHOLE (UNII: 56UJF6417L)
- EPIMEDIUM BREVICORNU WHOLE (UNII: 56UJF6417L) (Active Moiety)
Which are Delay Sprays For External-use 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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CROCIN (UNII: 877GWI46C2)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- WATER (UNII: 059QF0KO0R)
- OSTHOL (UNII: XH1TI1759C)
- METHOXSALEN (UNII: U4VJ29L7BQ)
- GARDENOSIDE (UNII: INE79XNR2C)
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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".