NDC 59886-414 Pure Baby Diaper Rash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59886 - Fischer Pharmaceuticals Ltd
- 59886-414 - Pure Baby Diaper Rash
Product Packages
NDC Code 59886-414-32
Package Description: 113 g in 1 TUBE
Product Details
What is NDC 59886-414?
What are the uses for Pure Baby Diaper Rash?
Which are Pure Baby Diaper Rash UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Pure Baby Diaper Rash 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:
- LEVOMENOL (UNII: 24WE03BX2T)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- DUNALIELLA SALINA (UNII: F4O1DKI9A6)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLOBULARIA CORDIFOLIA WHOLE (UNII: SD327VQ78H)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ALMOND OIL (UNII: 66YXD4DKO9)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TOCOPHEROL (UNII: R0ZB2556P8)
- WATER (UNII: 059QF0KO0R)
* 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".