NDC 50066-019 Scar Cream Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 50066-019?
What are the uses for Scar Cream Spf 30?
Which are Scar Cream Spf 30 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 Scar Cream Spf 30 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:
- EDETIC ACID (UNII: 9G34HU7RV0)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- MATRICARIA RECUTITA LEAF (UNII: 6I9LN466F0)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIMETHICONE 200 (UNII: RGS4T2AS00)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- WATER (UNII: 059QF0KO0R)
- ONION (UNII: 492225Q21H)
- SORBITOL (UNII: 506T60A25R)
- POLYESTER-7 (UNII: 0841698D2F)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ALLANTOIN (UNII: 344S277G0Z)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GARDEN CRESS SPROUT (UNII: PWQ18YNR62)
- GLYCERIN (UNII: PDC6A3C0OX)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TROLAMINE (UNII: 9O3K93S3TK)
- JOJOBA OIL (UNII: 724GKU717M)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
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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".