NDC 47993-215 Sun Block Sprary
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 47993-215-01
Package Description: 10 g in 1 BOTTLE
NDC Code 47993-215-02
Package Description: 15 g in 1 BOTTLE
NDC Code 47993-215-03
Package Description: 30 g in 1 BOTTLE
NDC Code 47993-215-04
Package Description: 50 g in 1 BOTTLE
NDC Code 47993-215-05
Package Description: 60 g in 1 BOTTLE
NDC Code 47993-215-06
Package Description: 80 g in 1 BOTTLE
NDC Code 47993-215-07
Package Description: 100 g in 1 BOTTLE
NDC Code 47993-215-08
Package Description: 100 g in 1 BOTTLE
Product Details
What is NDC 47993-215?
What are the uses for Sun Block Sprary?
Which are Sun Block Sprary UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Sun Block Sprary 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:
- CYCLOMETHICONE (UNII: NMQ347994Z)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- CARBOMER 1342 (UNII: 809Y72KV36)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- 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".