NDC 0363-9688 Walgreens Anti-sagging And Ultra Hydrating Day Broad Spectrum Spf15 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 0363-9688?
What are the uses for Walgreens Anti-sagging And Ultra Hydrating Day Broad Spectrum Spf15 Sunscreen?
Which are Walgreens Anti-sagging And Ultra Hydrating Day 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Walgreens Anti-sagging And Ultra Hydrating Day 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- MINERAL OIL (UNII: T5L8T28FGP)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
- PEG-100 STEARATE (UNII: YD01N1999R)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PALMITIC ACID (UNII: 2V16EO95H1)
- SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PEG-20 STEARATE (UNII: NBX892EA57)
- MANNITOL (UNII: 3OWL53L36A)
- YEAST (UNII: 3NY3SM6B8U)
- SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)
- PANTHENOL (UNII: WV9CM0O67Z)
- HYDROLYZED ELASTIN, BOVINE, ALKALINE (1000 MW) (UNII: ZR28QKN0WT)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- TROLAMINE (UNII: 9O3K93S3TK)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ALLANTOIN (UNII: 344S277G0Z)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SOY STEROL (UNII: PL360EPO9J)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- HONEY (UNII: Y9H1V576FH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BOVINE TYPE I COLLAGEN (UNII: FHJ3ATL51C)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SERINE (UNII: 452VLY9402)
- GLYCOGEN (UNII: 309GSC92U1)
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[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".