NDC 50760-8051 Denino Diaper Rash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50760 - Corpsain Sa De Cv
- 50760-8051 - Denino Diaper Rash
Product Packages
NDC Code 50760-8051-6
Package Description: 60 mL in 1 BOTTLE
Product Details
What is NDC 50760-8051?
What are the uses for Denino Diaper Rash?
Which are Denino 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)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) (Active Moiety)
- LANOLIN (UNII: 7EV65EAW6H)
- LANOLIN (UNII: 7EV65EAW6H) (Active Moiety)
Which are Denino 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:
- PETROLATUM (UNII: 4T6H12BN9U)
- WAX, YELLOW (UNII: 2ZA36H0S2V)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
* 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".