NDC 70116-001 Eezy Sun Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70116 - Bio Earth Manufacturing (pty) Ltd
- 70116-001 - Eezy Sun Spf 30
Product Packages
NDC Code 70116-001-01
Package Description: 8 mL in 1 POUCH
Product Details
What is NDC 70116-001?
Which are Eezy Sun Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- MERADIMATE (UNII: J9QGD60OUZ)
- MERADIMATE (UNII: J9QGD60OUZ) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Eezy Sun Spf 30 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:
- BULBINE FRUTESCENS WHOLE (UNII: M2U1C7UW6Y)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- VITAMIN A (UNII: 81G40H8B0T)
- WATER (UNII: 059QF0KO0R)
- PETROLATUM (UNII: 4T6H12BN9U)
- XANTHAN GUM (UNII: TTV12P4NEE)
* 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".