NDC 42421-814 H-e-b Skin Corrective Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen Light/medium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42421 - Emilia Personal Care Inc.
- 42421-814 - H-e-b Skin Corrective Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen Light/medium
Product Packages
NDC Code 42421-814-11
Package Description: 1 TUBE in 1 CARTON / 75 mL in 1 TUBE
Product Details
What is NDC 42421-814?
What are the uses for H-e-b Skin Corrective Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen Light/medium?
Which are H-e-b Skin Corrective Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen Light/medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are H-e-b Skin Corrective Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen Light/medium 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)
- MICA (UNII: V8A1AW0880)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- ALCOHOL (UNII: 3K9958V90M)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- KAOLIN (UNII: 24H4NWX5CO)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- NYLON-12 (UNII: 446U8J075B)
- FERROUS OXIDE (UNII: G7036X8B5H)
- TROLAMINE (UNII: 9O3K93S3TK)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALLANTOIN (UNII: 344S277G0Z)
- CAFFEINE (UNII: 3G6A5W338E)
- HYDROXYETHYL CELLULOSE (5500 MPA.S AT 2%) (UNII: M825OX60H9)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- HYALURONIC ACID (UNII: S270N0TRQY)
* 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".