NDC 57650-159 Samhealthyskin B.b. Sunscreen Broad Spectrum Spf 40
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 57650-159?
What are the uses for Samhealthyskin B.b. Sunscreen Broad Spectrum Spf 40?
Which are Samhealthyskin B.b. Sunscreen Broad Spectrum Spf 40 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Samhealthyskin B.b. Sunscreen Broad Spectrum Spf 40 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYETHYLENE GLYCOL 500 (UNII: 761NX2Q08Y)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- TALC (UNII: 7SEV7J4R1U)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYALURONIC ACID (UNII: S270N0TRQY)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- SHEA BUTTER (UNII: K49155WL9Y)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALLANTOIN (UNII: 344S277G0Z)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- LICORICE (UNII: 61ZBX54883)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
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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".