NDC 41250-794 Sunscreen Spf 30 Meijer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 41250-794?
Which are Sunscreen Spf 30 Meijer 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Sunscreen Spf 30 Meijer 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:
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SHEA BUTTER (UNII: K49155WL9Y)
- PAPAYA (UNII: KU94FIY6JB)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- COCO GLUCOSIDE (UNII: ICS790225B)
- COLOCASIA ESCULENTA ROOT (UNII: H7B71Q0G0D)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- 2-ETHYLHEXYL BENZOATE (UNII: R63ZWW1A13)
- GLYCERIN (UNII: PDC6A3C0OX)
- MANGO (UNII: I629I3NR86)
- MANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MICA (UNII: V8A1AW0880)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- PANTHENOL (UNII: WV9CM0O67Z)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P)
- PLUMERIA RUBRA FLOWER (UNII: 8P7XXY759H)
- PROPANEDIOL (UNII: 5965N8W85T)
- PROPYLENE GLYCOL DIBENZOATE (UNII: EQY32Z1AN4)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- GUAVA (UNII: 74O70D6VG0)
- JOJOBA BUTTER (UNII: XIA46H803R)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)
- WATER (UNII: 059QF0KO0R)
- 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".