NDC 62802-104 Parrot Head Floridays Face 50
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62802-104?
What are the uses for Parrot Head Floridays Face 50?
Which are Parrot Head Floridays Face 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Parrot Head Floridays Face 50 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)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- PROPANEDIOL (UNII: 5965N8W85T)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SQUALANE (UNII: GW89575KF9)
- XANTHAN GUM (UNII: TTV12P4NEE)
- WATERMELON (UNII: 231473QB6R)
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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".