NDC 66163-2613 Sharx - Sunbreaker Moisturizing Sunscreen Spf55 Broad Spectrum
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 66163-2613?
What are the uses for Sharx - Sunbreaker Moisturizing Sunscreen Spf55 Broad Spectrum?
Which are Sharx - Sunbreaker Moisturizing Sunscreen Spf55 Broad Spectrum UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sharx - Sunbreaker Moisturizing Sunscreen Spf55 Broad Spectrum 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)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- SORBITOL (UNII: 506T60A25R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- ALCOHOL (UNII: 3K9958V90M)
- OCTISALATE (UNII: 4X49Y0596W)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BETULA PUBESCENS BARK (UNII: 3R504894L9)
- GARDEN CRESS SPROUT (UNII: PWQ18YNR62)
- SAGE (UNII: 065C5D077J)
- COLA ACUMINATA SEED (UNII: 1F8VIW1479)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ISOMALT (UNII: S870P55O2W)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".