NDC 11727-006 X-pel Anti-lice
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11727 - Dermedics Laboratories
- 11727-006 - X-pel Anti-lice
Product Packages
NDC Code 11727-006-06
Package Description: 170 g in 1 BOTTLE
Product Details
What is NDC 11727-006?
What are the uses for X-pel Anti-lice?
Which are X-pel Anti-lice UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
Which are X-pel Anti-lice 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PYROLIGNEOUS ACID (UNII: N4G9GAT76C)
- AMODIMETHICONE (1300 CST) (UNII: 3V7U636DWN)
- NONOXYNOL-10 (UNII: K7O76887AP)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE SODIUM (UNII: MP1J8420LU)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
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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".