NDC 49738-626 Daily Moisturizing Broad Spectrum Spf15 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49738 - Kmart Corporation
- 49738-626 - Daily Moisturizing Broad Spectrum Spf15 Sunscreen
Product Packages
NDC Code 49738-626-11
Package Description: 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Details
What is NDC 49738-626?
What are the uses for Daily Moisturizing Broad Spectrum Spf15 Sunscreen?
Which are Daily Moisturizing Broad Spectrum Spf15 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Daily Moisturizing Broad Spectrum Spf15 Sunscreen 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- PANTHENOL (UNII: WV9CM0O67Z)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
- DOCOSANOL (UNII: 9G1OE216XY)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PEG-4 DILAURATE (UNII: KCR71CW036)
- PEG-100 STEARATE (UNII: YD01N1999R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
* 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".